ABX Micros 60 OT

ABX Micros 60 (O.T.B.)

Registry build 21.09.26
3manufacturers in China registered for this device type
1catalogue number
6510(k) clearances naming this product code

Who Else Makes It

Concentrated in Guangdong (2), Jiangsu (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code GKZ
Manufacturer City Province Registered as Device types
VTech Communications Ltd Dongguan Guangdong Contract manufacturer 5
Shenzhen Mindray BIO-Medical Electronics Co., Ltd. Shenzhen Guangdong Specification developer 61
Onechipdx Biotech (Suzhou) Co., Ltd. Suzhou Jiangsu Specification developer 2

Record

Regulatory record for ABX Micros 60 OT
Listed by Horiba ABX SAS, France
FDA product code GKZ
Device type Counter, Differential Cell
Device class Class 2
Regulation 21 CFR 864.5220
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K030799
Record published 2016-09-02
Record revised 2024-05-16 (version 6)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Label carries serial number

Catalogue Numbers

Catalogue numbers for ABX Micros 60 OT
Catalogue number Size Status
1280070125, 1280070126 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
QBC Diagnostics Drucker Diagnostics, LLC 41
Cell-DYN Abbott Laboratories 19
Research and Diagnostic Systems Research AND Diagnostic Systems, Inc. 17
Simultest Becton, Dickinson AND Company 10
BD FACSCanto™ Becton, Dickinson AND Company 10
FACSCanto Becton, Dickinson AND Company 7
BD Multitest Becton, Dickinson AND Company 6
Coulter AcT Beckman Coulter, Inc. 6
BD™ Multi-Check Becton, Dickinson AND Company 6
BD Tritest Becton, Dickinson AND Company 6
Coulter LH Beckman Coulter, Inc. 5
HemoScreen Pixcell Medical Inc. 5

Showing 12 of 245. All products under Counter, Differential Cell

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K232946 2024-05-21
K170353 2017-11-01
K151133 2015-12-09
K141161 2014-12-20
K053308 2005-12-29
K050719 2005-04-26

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