Herbert Stanley Co.
Country not established
- Devices
- 2
What Herbert Stanley Co. makes
Herbert Stanley Co. manufactures electrode gel and ultrasonic transmission gel, which are used to enhance conductivity and acoustic coupling in medical diagnostic and therapeutic procedures.
These products are classified as Class II devices under FDA regulations and are supported by 510(k) clearances. The company is based in the United States.
Catalogue
Electrode Gel Ref K884504
Regimes: 510(k) Registry: 510(k)Ultrasonic Transmission Gel Ref K884503
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Herbert Stanley Co. have in the registry?
The registry currently lists 2 devices for Herbert Stanley Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Herbert Stanley Co.'s devices?
Among its 2 most recently registered devices, Herbert Stanley Co. has devices listed in FDA 510(k) (2 devices).
What risk classes do Herbert Stanley Co.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Herbert Stanley Co.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Herbert Stanley Co. in the registry?
The most recently registered devices listed for Herbert Stanley Co. include ELECTRODE GEL and ULTRASONIC TRANSMISSION GEL.