Hill-Med, Inc.
United StatesFDA applicant, unverified
- Devices
- 10
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Hm-880 I Ref K932817
Regimes: 510(k) Registry: 510(k)Hm-930 Electrosurgical Unit Ref K993991
Regimes: 510(k) Registry: 510(k)Hm-0660 Ref K932782
Regimes: 510(k) Registry: 510(k)Hm-0690 Colposcope Ref K932896
Regimes: 510(k) Registry: 510(k)Hm-0970 Ref K932720
Regimes: 510(k) Registry: 510(k)Hm-88011 Solid State Electr Surgical Unit Ref K961473
Regimes: 510(k) Registry: 510(k)Hm-Spiro Ref K951718
Regimes: 510(k) Registry: 510(k)Hm-880 Ref K932818
Regimes: 510(k) Registry: 510(k)Hm-Cryo Ref K940140
Regimes: 510(k) Registry: 510(k)Electrosurgical Unit Ref K981781
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hill-Med, Inc. have in the registry?
The registry currently lists 10 devices for Hill-Med, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hill-Med, Inc.'s devices?
Among its 10 most recently registered devices, Hill-Med, Inc. has devices listed in FDA 510(k) (10 devices).
What risk classes do Hill-Med, Inc.'s devices fall under?
Among its 10 most recently registered devices, the classes recorded for Hill-Med, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hill-Med, Inc. in the registry?
The most recently registered devices listed for Hill-Med, Inc. include HM-880 I, HM-930 ELECTROSURGICAL UNIT, HM-0660 and HM-0690 COLPOSCOPE.