Medevice, Inc.
Country not established
- Devices
- 6
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Mede-Flo I.V. Extension Set Ref K912856
Regimes: 510(k) Registry: 510(k)Bio-Mate(Tm) Epidural Catheter Ref K884969
Regimes: 510(k) Registry: 510(k)E-Pulse Ref K091875
Regimes: 510(k) Registry: 510(k)Sightsure Operational Indicator, Model SS301 Ref K072550
Regimes: 510(k) Registry: 510(k)Bio-Mate(Tm) Pediatric Epidural Catheter Ref K901129
Regimes: 510(k) Registry: 510(k)Bio-Mate Pic Catheter Ref K920638
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medevice, Inc. have in the registry?
The registry currently lists 6 devices for Medevice, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medevice, Inc.'s devices?
Among its 6 most recently registered devices, Medevice, Inc. has devices listed in FDA 510(k) (6 devices).
What risk classes do Medevice, Inc.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Medevice, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medevice, Inc. in the registry?
The most recently registered devices listed for Medevice, Inc. include MEDE-FLO I.V. EXTENSION SET, BIO-MATE(TM) EPIDURAL CATHETER, E-PULSE and SIGHTSURE OPERATIONAL INDICATOR, MODEL SS301.