Westmark Enterprises, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Westmark Enterprises, Inc. makes
Westmark Enterprises, Inc. manufactures barrier devices for cardiopulmonary resuscitation, including the Modified C.P.R. MicroShield, which protects rescuers during chest compressions, and plastic mouth barrier devices designed to prevent transmission of HSV-I and HCV-E during rescue breathing.
These products are classified as Class I medical devices under FDA regulations and are supported by 510(k) clearances. The company is based in the United States.
Catalogue
Modified C.P.R. Microshield Ref K871403
Regimes: 510(k) Registry: 510(k)Plastic Mouth Barrier Hsv-I Ref K853266
Regimes: 510(k) Registry: 510(k)Plastic Mouth Barrier Hcv-E Ref K860780
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Westmark Enterprises, Inc. have in the registry?
The registry currently lists 3 devices for Westmark Enterprises, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Westmark Enterprises, Inc.'s devices?
Among its 3 most recently registered devices, Westmark Enterprises, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Westmark Enterprises, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Westmark Enterprises, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Westmark Enterprises, Inc. in the registry?
The most recently registered devices listed for Westmark Enterprises, Inc. include MODIFIED C.P.R. MICROSHIELD, PLASTIC MOUTH BARRIER HSV-I and PLASTIC MOUTH BARRIER HCV-E.