Ash Medical Systems, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Modified Bio. Hemodialysis & Hd-1000 Disp. Cart. Ref K870270
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ash Medical Systems, Inc. have in the registry?
The registry currently lists 3 devices for Ash Medical Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ash Medical Systems, Inc.'s devices?
Among its 3 most recently registered devices, Ash Medical Systems, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Ash Medical Systems, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Ash Medical Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ash Medical Systems, Inc. in the registry?
The most recently registered devices listed for Ash Medical Systems, Inc. include MODIFIED BIO. HEMODIALYSIS & HD-1000 DISP. CART., BIOLOGIC 1000 HEMODIALYSIS MACH/HD-1000 DISP CARTR and MODIFIED BIOLOGIC 1000 HEMODIAL. & HD-1000 DIS CAR.