Pulse Med, Inc.
Country not established
- Devices
- 1
What Pulse Med, Inc. makes
Pulse Med, Inc. manufactures custom packaging and procedural trays designed for use in operating rooms, providing sterile and organized supplies for surgical procedures.
These products are classified as Class II medical devices under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pulse Med, Inc. have in the registry?
The registry currently lists 1 device for Pulse Med, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pulse Med, Inc.'s devices?
Among its 1 most recently registered device, Pulse Med, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Pulse Med, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Pulse Med, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pulse Med, Inc. in the registry?
The most recently registered devices listed for Pulse Med, Inc. include PULSE MED CUSTOM PKG. PROC. TRAYS OPERATING ROOMS.