C015

Interventional fluoroscopic x-ray system for processing and real-time treatment of fluoroscopic images

Registry build 21.09.26
5manufacturers in China registered for this device type
2catalogue numbers in this listing
1510(k) clearance

Who Else Makes It

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

Chinese manufacturers registered for FDA product code OWB
Manufacturer City Province Registered as Device types
GE Hangwei Medical Systems Co., Ltd. Beijing Beijing Specification developer 22
GE Healthcare (China) Co., Ltd. Beijing Beijing Specification developer 22
Shanghai United Imaging Healthcare Co., Ltd. Shanghai Shanghai Manufacturer 12
Siemens Shanghai, Medical Equipment Ltd. Shanghai Shanghai Contract manufacturer 10
Siemens Shenzhen Magnetic Resonance Ltd. Shenzhen Guangdong Contract manufacturer 8

Record

Regulatory record for C015
Listed by Micronica Srl, Italy
FDA product code OWB
Device type Interventional Fluoroscopic X-Ray System
Device class Class 2
Regulation 21 CFR 892.1650
510(k) K192182
Record published 2020-03-16

Specifications

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

Catalogue Numbers

Catalogue numbers for C015
Catalogue number Size Status
FP XL C015 In distribution
FP XS C015 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
TrackX Trackx Technology Inc. 86
Trinias Shimadzu Corp. 54
Allura Xper FD Philips Medical Systems Nederland B.V. 21
Azurion Philips Medical Systems Nederland B.V. 19
LessRay Nuvasive, Inc. 16
Intelli-C Accessory Nrt – Nordisk Røntgen Teknik A/S 13
Pulse Nuvasive, Inc. 12
O-ARM® Medtronic Navigation, Inc. 11
Genoray Genoray Co., Ltd. 10
Fujifilm Healthcare Americas Corporation A.T.S. Applicazione Tecnologie Speciali SRL 7
Fujifilm Medical Systems U.S.A. Inc. A.T.S. Applicazione Tecnologie Speciali SRL 6
Stephanix A.T.S. Applicazione Tecnologie Speciali SRL 6

Showing 12 of 122. All products under Interventional Fluoroscopic X-Ray System

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K192182 2020-01-17

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