Raymart Development Co.
Country not established
- Devices
- 1
What Raymart Development Co. makes
Raymart Development Co. manufactures AMNIPERF™, a Class I medical device designed for amniotic fluid perfusion monitoring during pregnancy.
The device is regulated under the FDA’s 510(k) pathway and is listed in the U.S. regulatory database. The company is based in the United States.
Catalogue
Amniperf(Tm) Ref K926425
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Raymart Development Co. have in the registry?
The registry currently lists 1 device for Raymart Development Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Raymart Development Co.'s devices?
Among its 1 most recently registered device, Raymart Development Co. has devices listed in FDA 510(k) (1 device).
What risk classes do Raymart Development Co.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Raymart Development Co.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Raymart Development Co. in the registry?
The most recently registered devices listed for Raymart Development Co. include AMNIPERF(TM).