FACSVia

BD FACSVia™ Clinical Software, Test Definitions, and Documentation v1.2

Registry build 21.09.26
1manufacturer
2catalogue numbers in this listing
2510(k) clearances naming this product code

Who Else Makes It

Registered in Jiangsu.

Chinese manufacturers registered for FDA product code OYE
Manufacturer City Province Registered as Device types
Beckman Coulter Biotechnology (Suzhou) Co., Ltd. Suzhou Jiangsu Specification developer 2

Record

Regulatory record for FACSVia
Listed by Becton, Dickinson AND Company, United States
FDA product code OYE
Device type Flow Cytometric Reagents And Accessories.
Device class Class 2
Regulation 21 CFR 864.5220
Establishment Contract manufacturer, Contract steriliser, Specification developer, Repacker / relabeller, Manufacturer
Record published 2017-05-23
Record revised 2024-10-22 (version 9)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries lot or batch number, manufacturing date, serial number
Storage Special storage condition: Room Temperature
Distribution end date 2023-02-16

Catalogue Numbers

Catalogue numbers for FACSVia
Catalogue number Size Status
660561 In distribution
662386 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Navios EX Beckman Coulter Ireland Inc 7
BD FACSuite Becton, Dickinson AND Company 5
BD FACSLyric Becton, Dickinson AND Company 4
FACSCanto Becton, Dickinson AND Company 4
Navios Analysis Software Beckman Coulter Ireland Inc 3
FACSuite Becton, Dickinson AND Company 3
Flow Cytometric Reagents And Accessories. Becton, Dickinson AND Company 3
BD FACSDiva Becton, Dickinson AND Company 3
Navios Beckman Coulter Ireland Inc 3
BD FACSDiva™ Becton, Dickinson AND Company 2
Navios tetra Software Beckman Coulter Ireland Inc 1
DxFLEX Beckman Coulter, Inc. 1

Showing 12 of 20. All products under Flow Cytometric Reagents And Accessories.

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K201814 2020-09-28
K170974 2017-07-03

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