Pirdy, Inc.
Country not established
- Devices
- 1
What Pirdy, Inc. makes
Pirdy, Inc. manufactures the PIRD-Y medical device, which is classified as a Class II product.
The PIRD-Y is regulated under the FDA 510(k) pathway and is listed in the FDA 510(k) registry. Pirdy, Inc. is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Pird-Y Ref K842262
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pirdy, Inc. have in the registry?
The registry currently lists 1 device for Pirdy, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pirdy, Inc.'s devices?
Among its 1 most recently registered device, Pirdy, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Pirdy, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Pirdy, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pirdy, Inc. in the registry?
The most recently registered devices listed for Pirdy, Inc. include PIRD-Y.