Merced Medical, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 3002902165
- Devices
- 5
- Registrations
- FDA
- FDA recalls
- 0
What Merced Medical, Inc. makes
Merced Medical, Inc. manufactures manual resuscitation devices, including CPR bags and MER bags for emergency airway management, as well as electro-surgical units for tissue ablation procedures. Their product line also includes a percussor device for chest physiotherapy and a thermoprobe for temperature monitoring in medical procedures.
The company’s devices are classified under FDA Class II and are listed via 510(k) premarket notifications. These products are regulated under US medical device laws and are intended for commercial distribution within the United States.
Catalogue
Cpr Bag Ref K911622
Regimes: 510(k) Registry: 510(k)Thermoprobe 210 Ref K900569
Regimes: 510(k) Registry: 510(k)Ley Electro-Surgical Units Ref K790642
Regimes: 510(k) Registry: 510(k)Mj Percussor(Tm) Ref K901026
Regimes: 510(k) Registry: 510(k)Mer Bag Ref K915810
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3002902165
- Address
- 9217 E Verde Grove Vw, Scottsdale, AZ, 85255
Frequently asked questions
How many devices does Merced Medical, Inc. have in the registry?
The registry currently lists 5 devices for Merced Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Merced Medical, Inc.'s devices?
Among its 5 most recently registered devices, Merced Medical, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Merced Medical, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Merced Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Merced Medical, Inc. in the registry?
The most recently registered devices listed for Merced Medical, Inc. include CPR BAG, THERMOPROBE 210, LEY ELECTRO-SURGICAL UNITS and MJ PERCUSSOR(TM).