Fia Man Co.
Country not established
- Devices
- 1
What Fia Man Co. makes
Fia Man Co. manufactures the MICROPAD, a reusable, disposable, or single-use medical device designed for precise fluid sampling or administration in clinical settings.
The MICROPAD is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Micropad Ref K823301
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Fia Man Co. have in the registry?
The registry currently lists 1 device for Fia Man Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Fia Man Co.'s devices?
Among its 1 most recently registered device, Fia Man Co. has devices listed in FDA 510(k) (1 device).
What risk classes do Fia Man Co.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Fia Man Co.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Fia Man Co. in the registry?
The most recently registered devices listed for Fia Man Co. include MICROPAD.