Pluromed, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Backstop And Backstop Injector Ref K090430
Regimes: 510(k) Registry: 510(k)Backstop Catheter Ref K110491
Regimes: 510(k) Registry: 510(k)Backstop Catheter Ref K103349
Regimes: 510(k) Registry: 510(k)Backstop Catheter, Model 60-0000-3100 Ref K090270
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pluromed, Inc. have in the registry?
The registry currently lists 4 devices for Pluromed, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pluromed, Inc.'s devices?
Among its 4 most recently registered devices, Pluromed, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Pluromed, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Pluromed, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pluromed, Inc. in the registry?
The most recently registered devices listed for Pluromed, Inc. include BACKSTOP AND BACKSTOP INJECTOR, BACKSTOP CATHETER and BACKSTOP CATHETER, MODEL 60-0000-3100.