W. Murphy Ent., Inc.
CanadaFDA 510(k) applicant, unverified
- Devices
- 3
What W. Murphy Ent., Inc. makes
W. Murphy Ent., Inc. manufactures portable rescue stretchers, including the WEEVAC 1, WEEVAC 6 infant evacuation stretcher, and the WEEVAC TC hand-carried rescue stretcher.
These devices are classified as Class I medical devices and are listed in the FDA 510(k) database. The company is based in the United States.
Catalogue
Weevac 1 Portable Rescue Stretcher Ref K902474
510(k) 510(k)Weevac 6 Infant Evacuation Stretcher Ref K902521
510(k) 510(k)Weevac Tc Hand Carried Rescue Stretcher Ref K910709
510(k) 510(k)
Frequently asked questions
How many devices does W. Murphy Ent., Inc. have in the registry?
The registry currently lists 3 devices for W. Murphy Ent., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list W. Murphy Ent., Inc.'s devices?
Among its 3 most recently registered devices, W. Murphy Ent., Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do W. Murphy Ent., Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for W. Murphy Ent., Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from W. Murphy Ent., Inc. in the registry?
The most recently registered devices listed for W. Murphy Ent., Inc. include WEEVAC 1 PORTABLE RESCUE STRETCHER, WEEVAC 6 INFANT EVACUATION STRETCHER and WEEVAC TC HAND CARRIED RESCUE STRETCHER.