Mcvicar Enterprises, Ltd.
CanadaFDA applicant, unverified
- Devices
- 1
What Mcvicar Enterprises, Ltd. makes
Mcvicar Enterprises, Ltd. manufactures The Waverly Wedge™ Inflatable Air Cushion, a Class I medical device designed to provide pressure redistribution and support for patient positioning, particularly in clinical or home care settings.
The company’s portfolio is regulated under FDA 510(k) clearance as a Class I device and is listed in the U.S. regulatory database. The manufacturer is based in the United States.
Catalogue
The Waverly Wedge(Tm) Inflatable Air Cushion Ref K895444
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mcvicar Enterprises, Ltd. have in the registry?
The registry currently lists 1 device for Mcvicar Enterprises, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mcvicar Enterprises, Ltd.'s devices?
Among its 1 most recently registered device, Mcvicar Enterprises, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Mcvicar Enterprises, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Mcvicar Enterprises, Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Mcvicar Enterprises, Ltd. in the registry?
The most recently registered devices listed for Mcvicar Enterprises, Ltd. include THE WAVERLY WEDGE(TM) INFLATABLE AIR CUSHION.