Mega-Tech Intl., Inc.
Country not established
- Devices
- 1
What Mega-Tech Intl., Inc. makes
Mega-Tech Intl., Inc. manufactures the FLOCARE device, a Class I medical product designed for fluid management or drainage applications in clinical settings.
The FLOCARE device is regulated under the FDA’s 510(k) pathway as a Class I product and is listed in the U.S. regulatory database. The company is based in the United States.
Catalogue
Flocare Ref K893875
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mega-Tech Intl., Inc. have in the registry?
The registry currently lists 1 device for Mega-Tech Intl., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mega-Tech Intl., Inc.'s devices?
Among its 1 most recently registered device, Mega-Tech Intl., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Mega-Tech Intl., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Mega-Tech Intl., Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Mega-Tech Intl., Inc. in the registry?
The most recently registered devices listed for Mega-Tech Intl., Inc. include FLOCARE.