Appriva Medical, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Appriva Medical, Inc. makes
Appriva Medical specializes in transseptal sheaths and transition catheters designed for cardiac procedures, including modified versions of the X-Sept Transseptal Sheath and associated dilator catheters for use in interventional cardiology.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearances. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Appriva Medical, Inc. have in the registry?
The registry currently lists 2 devices for Appriva Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Appriva Medical, Inc.'s devices?
Among its 2 most recently registered devices, Appriva Medical, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Appriva Medical, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Appriva Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Appriva Medical, Inc. in the registry?
The most recently registered devices listed for Appriva Medical, Inc. include MODIFICATION TO: X-SEPT TRANSSEPTAL SHEALTH AND TRANSITION CATHETER (WITH DILATOR), MODELS PL-12-12-09, PL-12-12-10 and X-SEPT TRANSSEPTAL SHEATH AND TRANSITION CATHETER, MODEL MV-03-09-90, MV-03-10-90, MV-03-11-90, MV-03-09-120, MV-03-10-1.