McKesson

Heavy Duty Suction Machine

Registry build 21.09.26
5manufacturers in China registered for this device type
2catalogue numbers in this listing

Who Else Makes It

Concentrated in Guangdong (2), Shanghai (1), Jiangsu (1).

Chinese manufacturers registered for FDA product code JCX
Manufacturer City Province Registered as Device types
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Jiangsu Jumao X-Care Medical Equipment Co., Ltd. Danyang Jiangsu Contract manufacturer 37
Laerdal Medical (Suzhou) Co., Ltd. 215009 Suzhou Jiangsu Province Repacker / relabeller 12
Vega Technologies Inc. Dongguan Guangdong Repacker / relabeller 7
Foshan Care Medical Technology Co., Ltd. Foshan Guangdong Manufacturer 3

Record

Regulatory record for McKesson
Listed by Mckesson Medical-Surgical Inc.
FDA product code JCX
Device type Apparatus, Suction, Ward Use, Portable, Ac-Powered
Device class Class 2
Regulation 21 CFR 878.4780
510(k) K982304
Record published 2025-12-03

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Latex Labelled latex-free
Label carries lot or batch number, manufacturing date, serial number

Catalogue Numbers

Catalogue numbers for McKesson
Catalogue number Size Status
146-7325P-D In distribution
146-18600 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
DeVilbiss DeVilbiss Healthcare LLC. 35
Neptune Stryker GmbH 16
Apparatus, Suction, Ward Use, Portable, Ac-Powered Zimmer Orthopaedic Surgical Products 16
IntelliCart™ Zimmer Orthopaedic Surgical Products 13
Penumbra System Penumbra Inc. 8
Schuco Allied Medical LLC 7
Gomco Allied Medical LLC 7
Roscoe Medical Drive DeVilbiss Healthcare 5
Cliq Aspirator Anest Iwata Sparmax Co., Ltd. 5
Drive Drive DeVilbiss Healthcare 4
Truvic Generator Taiwan Biomaterial Company, Ltd. 4
Phantom Innovative Med, Inc. 4

Showing 12 of 65. All products under Apparatus, Suction, Ward Use, Portable, Ac-Powered

Recalls Naming This Product

4 recalls name this product by its own identifiers, the 510(k) it is cleared under.

Recalls naming the identifiers of McKesson
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
DeVilbiss Healthcare LLC. 510(k) number 2016-05-23 Class II Component design/selection A small percentage of units of 7305 Series Vacu-Aide Suction Units are experiencing premature failure during operation. 48 units 2017-05-30
EMG Technology Co., Ltd. 510(k) number 2014-08-03 Class II Nonconforming Material/Component suction canister lids may have occluded ports. 1452 2015-08-25
DeVilbiss Healthcare LLC. 510(k) number 2013-03-07 Class II Use error End users of the DeVilbiss Disposable Suction Container/Filter had exposed the bacterial filter cartridge to fluid, thereby occluding the filter and rendering it unusable. 112,849 2014-11-06
DeVilbiss Healthcare LLC. 510(k) number 2008-10-27 Not classified Device Design Improper suction: Regulator knob does not turn properly which can affect the suction level. 78 units 2012-09-25

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.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer