Mellen Air Mfg., Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Mellen Air Mfg., Inc. makes
Mellen Air Mfg., Inc. manufactures alternating pressure air flotation mattress systems, including the APREMA I and AREMA II models, designed for patient positioning and pressure redistribution in clinical settings.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Arema Ii Ref K961129
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mellen Air Mfg., Inc. have in the registry?
The registry currently lists 2 devices for Mellen Air Mfg., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mellen Air Mfg., Inc.'s devices?
Among its 2 most recently registered devices, Mellen Air Mfg., Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Mellen Air Mfg., Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Mellen Air Mfg., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mellen Air Mfg., Inc. in the registry?
The most recently registered devices listed for Mellen Air Mfg., Inc. include APREMA I - ALTERNATING PRESSURE AIR FLOTATION MATTRESS SYSTEM and AREMA II.