North American Marketing Corp.
Country not established
- Devices
- 1
What North American Marketing Corp. makes
North American Marketing Corp. manufactures the MEDI-KLEER, a medical device designed for [specific use not provided in data].
The MEDI-KLEER 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
Medi-Kleer Ref K904871
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does North American Marketing Corp. have in the registry?
The registry currently lists 1 device for North American Marketing Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list North American Marketing Corp.'s devices?
Among its 1 most recently registered device, North American Marketing Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do North American Marketing Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for North American Marketing Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from North American Marketing Corp. in the registry?
The most recently registered devices listed for North American Marketing Corp. include MEDI-KLEER.