Maet Industries, Inc.
CanadaFDA applicant, unverified
- Devices
- 1
What Maet Industries, Inc. makes
Maet Industries, Inc. manufactures the QUICKAIR CHOKE RELIEVER (Model 59-001A), a device designed to clear airway obstructions in emergency medical scenarios.
The QUICKAIR CHOKE RELIEVER is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Quickair Choke Reliever, Model 59-001A Ref DEN000004
Regimes: De Novo Registry: De Novo
Frequently asked questions
How many devices does Maet Industries, Inc. have in the registry?
The registry currently lists 1 device for Maet Industries, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Maet Industries, Inc.'s devices?
Among its 1 most recently registered device, Maet Industries, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Maet Industries, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Maet Industries, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Maet Industries, Inc. in the registry?
The most recently registered devices listed for Maet Industries, Inc. include QUICKAIR CHOKE RELIEVER, MODEL 59-001A.