Euro-Am Pharma, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What Euro-Am Pharma, Inc. makes
Euro-Am Pharma, Inc. manufactures the OPOMAT Manual Resuscitator Ventilator, a portable device designed for manual ventilation support, and the ACU-BAND Accupressure Wrist Band, a wristband intended for acupressure therapy.
The company’s products are regulated under FDA Class II and Class U device classifications, with submissions recorded in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
Opomat Manual Resuscitator Ventilator Ref K912620
510(k) 510(k)Acu-Band Accupressure Wrist Band Ref K900588
510(k) 510(k)
Frequently asked questions
How many devices does Euro-Am Pharma, Inc. have in the registry?
The registry currently lists 2 devices for Euro-Am Pharma, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Euro-Am Pharma, Inc.'s devices?
Among its 2 most recently registered devices, Euro-Am Pharma, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Euro-Am Pharma, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Euro-Am Pharma, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Euro-Am Pharma, Inc. in the registry?
The most recently registered devices listed for Euro-Am Pharma, Inc. include OPOMAT MANUAL RESUSCITATOR VENTILATOR and ACU-BAND ACCUPRESSURE WRIST BAND.