Fiegert, Inc.
Country not established
- Devices
- 1
What Fiegert, Inc. makes
Fiegert, Inc. manufactures the Fiegert Endotech Cystoscope, a medical device used for visual inspection of the urinary bladder and lower urinary tract.
The Fiegert Endotech Cystoscope is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Fiegert Endotech Cystoscope Ref K970892
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Fiegert, Inc. have in the registry?
The registry currently lists 1 device for Fiegert, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Fiegert, Inc.'s devices?
Among its 1 most recently registered device, Fiegert, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Fiegert, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Fiegert, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Fiegert, Inc. in the registry?
The most recently registered devices listed for Fiegert, Inc. include FIEGERT ENDOTECH CYSTOSCOPE.