Hursch Ent., Inc.
Country not established
- Devices
- 1
What Hursch Ent., Inc. makes
Hursch Ent., Inc. manufactures the Berg Resuscitation Apparatus, a device designed for cardiopulmonary resuscitation (CPR) to assist in chest compressions during emergency cardiac care.
The Berg Resuscitation Apparatus is classified as a Class II medical device in the U.S. and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
The Berg Resuscitation Apparatus Ref K882833
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hursch Ent., Inc. have in the registry?
The registry currently lists 1 device for Hursch Ent., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hursch Ent., Inc.'s devices?
Among its 1 most recently registered device, Hursch Ent., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Hursch Ent., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Hursch Ent., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hursch Ent., Inc. in the registry?
The most recently registered devices listed for Hursch Ent., Inc. include THE BERG RESUSCITATION APPARATUS.