Cordis Webster, Inc.
United StatesFDA applicant, unverified
- Devices
- 10
Catalogue
Cordis Wester Star Catheter Ref K954390
Regimes: 510(k) Registry: 510(k)Cordis Webster Ref-Star Ex Surface Reference Device Model's D-1204-01, -02, -03, And -04. Ref K980961
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cordis Webster, Inc. have in the registry?
The registry currently lists 10 devices for Cordis Webster, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cordis Webster, Inc.'s devices?
Among its 10 most recently registered devices, Cordis Webster, Inc. has devices listed in FDA 510(k) (10 devices).
What risk classes do Cordis Webster, Inc.'s devices fall under?
Among its 10 most recently registered devices, the classes recorded for Cordis Webster, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cordis Webster, Inc. in the registry?
The most recently registered devices listed for Cordis Webster, Inc. include CORDIS WESTER STAR CATHETER, CORDIS WEBSTER REF-STAR EX SURFACE REFERENCE DEVICE MODEL'S D-1204-01, -02, -03, AND -04., CORDIS WEBSTER FIXED CURVE CATHETERS, MODELS D-1124, D-1085 and CORIDIS WEBSTER DEFLECTABLE BRAIDED-TIP ELECTRODE CATHETER.