Goodman, Goodman & Goodman
Country not established
- Devices
- 1
What Goodman, Goodman & Goodman makes
Goodman, Goodman & Goodman manufactures the P.T. MACHINE, which is a Class II medical device.
The company is based in the US and the P.T. MACHINE is listed in the FDA 510(k) registry.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
P.T. Machine Ref K974626
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Goodman, Goodman & Goodman have in the registry?
The registry currently lists 1 device for Goodman, Goodman & Goodman. Devices recorded under merged duplicate company entries are counted once.
Which registries list Goodman, Goodman & Goodman's devices?
Among its 1 most recently registered device, Goodman, Goodman & Goodman has devices listed in FDA 510(k) (1 device).
What risk classes do Goodman, Goodman & Goodman's devices fall under?
Among its 1 most recently registered device, the classes recorded for Goodman, Goodman & Goodman's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Goodman, Goodman & Goodman in the registry?
The most recently registered devices listed for Goodman, Goodman & Goodman include P.T. MACHINE.