General Medical Products, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What General Medical Products, Inc. makes
General Medical Products, Inc. manufactures manual resuscitation devices, including the Bauman CPR/Respirator and Bauman CPR/Resuscitator, designed for use in emergency medical situations to assist with ventilation during cardiopulmonary resuscitation.
These devices are classified as Class II under FDA regulations and are listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Bauman Cpr/Respirator Ref K864308
Regimes: 510(k) Registry: 510(k)Bauman Cpr/Resuscitator Ref K904346
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does General Medical Products, Inc. have in the registry?
The registry currently lists 2 devices for General Medical Products, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list General Medical Products, Inc.'s devices?
Among its 2 most recently registered devices, General Medical Products, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do General Medical Products, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for General Medical Products, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from General Medical Products, Inc. in the registry?
The most recently registered devices listed for General Medical Products, Inc. include BAUMAN CPR/RESPIRATOR and BAUMAN CPR/RESUSCITATOR.