Can-Am Medical, Inc.
CanadaFDA applicant, unverified
- Devices
- 1
What Can-Am Medical, Inc. makes
Can-Am Medical, Inc. manufactures the C.P.R. Landmark, a device designed to assist in cardiopulmonary resuscitation (CPR) by providing visual feedback and guidance to improve compression depth and rate during resuscitation efforts.
The C.P.R. Landmark is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
C.P.R. Landmarc Ref K900415
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Can-Am Medical, Inc. have in the registry?
The registry currently lists 1 device for Can-Am Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Can-Am Medical, Inc.'s devices?
Among its 1 most recently registered device, Can-Am Medical, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Can-Am Medical, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Can-Am Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Can-Am Medical, Inc. in the registry?
The most recently registered devices listed for Can-Am Medical, Inc. include C.P.R. LANDMARC.