What is FDA product code EOQ?

A bronchoscope (flexible or rigid) and accessories is a tubular endoscopic device with any of a group of accessory devices which attach to the bronchoscope and is intended to examine or treat the larynx and tracheobronchial tree. If the device is reprocessed, reprocessing validation data for this device type must be included in a 510(k) submission. If the device is reusable, validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission (82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).

Ear Nose & Throat › SurgicalBronchoscope (Flexible Or Rigid)

OES Bronchofiberscope Olympus BF Type N20

Name: OES Bronchofiberscope Olympus BF Type N20
Brand: OES Bronchofiberscope Olympus BF Type N20

Catalogue number OLYMPUS BF TYPE N20, listed by Olympus Medical Systems Corp., Japan, under Bronchoscope (Flexible Or Rigid). 21 manufacturers in China are registered for this product code.

Registry build 21.09.26

21manufacturers in China registered for this device type

1catalogue number

19510(k) clearances naming this product code

Who Else Makes It

Concentrated in Guangdong (7), Zhejiang (5), Jiangsu (4). 5 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code EOQ
Manufacturer	City	Province	Registered as	Device types
Flexicare Medical (Dongguan) Ltd.	Dongguan	Guangdong	Contract manufacturer	48
Guangdong MacroLux Medical Technology Co., Ltd.	Dongguan	Guangdong	Contract manufacturer	9
Ningbo Wise Optomech Technology Corporation	Ningbo	Zhejiang	Contract manufacturer	4
Hangzhou Broncus Medical Co., Ltd.	Hangzhou	Zhejiang	Contract manufacturer	1
Tianjin Puli Ark Medical Technology Co., Ltd.	Dongli District	Tianjin	Contract manufacturer	1
Micro-Tech (Nanjing) Co., Ltd.	Nan Jing	Jiangsu	Contract manufacturer	49
Zhejiang Huanyi Sterilization Technology Co., Ltd.	Huzhou	Zhejiang	Contract manufacturer	25
Shenzhen Hugemed Medical Technical Development Co., Ltd.	Shenzhen	Guangdong	Manufacturer	22
Suzhou Prosteri Medical Technology Co., Ltd.	Suzhou	Jiangsu	Contract manufacturer	20
Suzhou Virgil Medical Technology Co., Ltd.	Suzhou	Jiangsu	Contract manufacturer	20
Scivita Medical Technology Co., Ltd.	Suzhou	Jiangsu	Manufacturer	19
Anrei Medical (Hangzhou) Co., Ltd.	Hangzhou	Zhejiang	Manufacturer	12

Showing 12 of 21. All 21 manufacturers in China registered for Bronchoscope (Flexible Or Rigid)

Record

Regulatory record for OES Bronchofiberscope Olympus BF Type N20
Listed by	Olympus Medical Systems Corp., Japan
FDA product code	EOQ
Device type	Bronchoscope (Flexible Or Rigid)
Device class	Class 2
Regulation	21 CFR 874.4680
Establishment	Specification developer, Manufacturer, Exporter
Record published	2022-07-25
Record revised	2025-11-24 (version 4)

Specifications

Specifications
MRI safety	Labeling does not contain MRI Safety Information
Label carries	manufacturing date, serial number

Catalogue Numbers

Catalogue numbers for OES Bronchofiberscope Olympus BF Type N20
Catalogue number	Size	Status
OLYMPUS BF TYPE N20		In distribution

Same Product Code

Other products under the same FDA product code
Product	Sold by	Catalogue numbers
Bronchoscope (Flexible Or Rigid)	Karl Storz GmbH & Co. KG	248
Pentax	Hoya Corporation	39
Biopsy Forceps	Olympus Medical Systems Corp.	31
Single-Use flexible Video Bronchoscope	Hunan Vathin Medical Instrument Co., Ltd.	27
Pilling	Teleflex Medical LLC	24
Silicone cap	Efer Endoscopy	22
Bronchoscope (Flexible Or Rigid)	Intuitive Surgical, Inc.	20
Endoso	Hunan Endoso Life Technology Co., Ltd.	20
Exalt ™	Boston Scientific Corporation	17
Grasping Forceps	Olympus Medical Systems Corp.	16
LungVision Tool	Body Vision Medical Ltd	16
Fujifilm	Fujifilm Corporation	15

Showing 12 of 255. All products under Bronchoscope (Flexible Or Rigid)

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance	Decision date
K252341	2026-04-23
K250862	2025-06-23
K250118	2025-06-04
K250957	2025-05-30
K222861	2023-06-15
K221631	2022-09-26
K212667	2021-09-22
K201300	2021-01-26
K201758	2021-01-21
K200342	2020-12-17
K200397	2020-04-24
K192164	2020-03-06
K183419	2019-09-05
K172726	2018-04-30
K121959	2013-01-10
K082720	2008-11-05
K061313	2006-08-31
K060243	2006-06-23
K050220	2005-02-10

Recalls Naming This Product

1 recall names this product by its own identifier, the UDI on its label.

Recalls naming the identifiers of OES Bronchofiberscope Olympus BF Type N20
Recalled by	Identified by	Initiated	FDA class	Root cause	Reason	Quantity
Olympus Corporation of the Americas	UDI-DI	2023-07-27	Class II	Labeling Change Control	Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.	881 units

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.