Equipement Biomedical Specialise, Inc.
CanadaFDA 510(k) applicant, unverified
- Devices
- 1
What Equipement Biomedical Specialise, Inc. makes
Equipement Biomedical Specialise, Inc. makes the REMUSK MP device.
The REMUSK MP is a Class II medical device listed in the FDA 510(k) registry, and the company is based in the United States.
Catalogue
Remusk Mp Ref K922029
510(k) 510(k)
Frequently asked questions
How many devices does Equipement Biomedical Specialise, Inc. have in the registry?
The registry currently lists 1 device for Equipement Biomedical Specialise, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Equipement Biomedical Specialise, Inc.'s devices?
Among its 1 most recently registered device, Equipement Biomedical Specialise, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Equipement Biomedical Specialise, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Equipement Biomedical Specialise, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Equipement Biomedical Specialise, Inc. in the registry?
The most recently registered devices listed for Equipement Biomedical Specialise, Inc. include REMUSK MP.