Microlab Americas, Inc.
Country not established
- Devices
- 1
What Microlab Americas, Inc. makes
Microlab Americas, Inc. manufactures ACTHYDERM, a topical formulation for diagnostic testing of adrenal function.
ACTHYDERM is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Acthyderm Ref K083016
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Microlab Americas, Inc. have in the registry?
The registry currently lists 1 device for Microlab Americas, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Microlab Americas, Inc.'s devices?
Among its 1 most recently registered device, Microlab Americas, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Microlab Americas, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Microlab Americas, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Microlab Americas, Inc. in the registry?
The most recently registered devices listed for Microlab Americas, Inc. include ACTHYDERM.