Klh Medical, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Patient Examination Gloves (Latex) Ref K891710
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Patient Examination Gloves (Latex) Ref K891851
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Klh Medical, Inc. have in the registry?
The registry currently lists 3 devices for Klh Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Klh Medical, Inc.'s devices?
Among its 3 most recently registered devices, Klh Medical, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Klh Medical, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Klh Medical, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Klh Medical, Inc. in the registry?
The most recently registered devices listed for Klh Medical, Inc. include PATIENT EXAMINATION GLOVES (LATEX) and LATEX PATIENT EXAMINATION GLOVES - HYPOALLERGENIC.