Corning Costar Corp.
United StatesFDA applicant, unverified
- Devices
- 8
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Serocluster Flexible Vinyl U & V Pl. Ref K803243
Regimes: 510(k) Registry: 510(k)U - Star (Micro-Star) Ref K860703
Regimes: 510(k) Registry: 510(k)Octapettes Ref K823137
Regimes: 510(k) Registry: 510(k)Serocluster Eia Plates Ref K803242
Regimes: 510(k) Registry: 510(k)Serocluster U And V Ref K800240
Regimes: 510(k) Registry: 510(k)Cell Scraper Ref K823138
Regimes: 510(k) Registry: 510(k)Cell Lifter Ref K871559
Regimes: 510(k) Registry: 510(k)Assay Strips Ref K803244
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Corning Costar Corp. have in the registry?
The registry currently lists 8 devices for Corning Costar Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Corning Costar Corp.'s devices?
Among its 8 most recently registered devices, Corning Costar Corp. has devices listed in FDA 510(k) (8 devices).
What risk classes do Corning Costar Corp.'s devices fall under?
Among its 8 most recently registered devices, the classes recorded for Corning Costar Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Corning Costar Corp. in the registry?
The most recently registered devices listed for Corning Costar Corp. include SEROCLUSTER FLEXIBLE VINYL U & V PL., U - STAR (MICRO-STAR), OCTAPETTES and SEROCLUSTER EIA PLATES.