Act Medical, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Flexneedle Plus Ref K990693
Regimes: 510(k) Registry: 510(k)Endoscopic Catheter Ref K953967
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Act Medical, Inc. have in the registry?
The registry currently lists 2 devices for Act Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Act Medical, Inc.'s devices?
Among its 2 most recently registered devices, Act Medical, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Act Medical, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Act Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Act Medical, Inc. in the registry?
The most recently registered devices listed for Act Medical, Inc. include FLEXNEEDLE PLUS and ENDOSCOPIC CATHETER.