Akron Catheter, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Akro-Sil Plus Ref K864736
Regimes: 510(k) Registry: 510(k)Kelly Inflatable T Drain Ref K823428
Regimes: 510(k) Registry: 510(k)Catheter, Natural Latex Urethral Ref K760440
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Akron Catheter, Inc. have in the registry?
The registry currently lists 3 devices for Akron Catheter, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Akron Catheter, Inc.'s devices?
Among its 3 most recently registered devices, Akron Catheter, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Akron Catheter, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Akron Catheter, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Akron Catheter, Inc. in the registry?
The most recently registered devices listed for Akron Catheter, Inc. include AKRO-SIL PLUS, KELLY INFLATABLE T DRAIN and CATHETER, NATURAL LATEX URETHRAL.