Mary M. Sorg (An Individual) Dba PJ Sleeper'S
Country not established
- Devices
- 1
What Mary M. Sorg (An Individual) Dba PJ Sleeper'S makes
Mary M. Sorg (DBA PJ Sleeper’s) manufactures a restless leg device, designed to address symptoms associated with restless legs syndrome.
The device is classified as Class I under FDA regulations and is listed in the FDA 510(k) registry. The manufacturer operates from the United States.
Catalogue
Restless Leg Device Ref DEN110009
Regimes: De Novo Registry: De Novo
Frequently asked questions
How many devices does Mary M. Sorg (An Individual) Dba PJ Sleeper'S have in the registry?
The registry currently lists 1 device for Mary M. Sorg (An Individual) Dba PJ Sleeper'S. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mary M. Sorg (An Individual) Dba PJ Sleeper'S's devices?
Among its 1 most recently registered device, Mary M. Sorg (An Individual) Dba PJ Sleeper'S has devices listed in FDA 510(k) (1 device).
What risk classes do Mary M. Sorg (An Individual) Dba PJ Sleeper'S's devices fall under?
Among its 1 most recently registered device, the classes recorded for Mary M. Sorg (An Individual) Dba PJ Sleeper'S's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Mary M. Sorg (An Individual) Dba PJ Sleeper'S in the registry?
The most recently registered devices listed for Mary M. Sorg (An Individual) Dba PJ Sleeper'S include RESTLESS LEG DEVICE.