Precision Endoscopy of America, Inc.
Country not established
- Devices
- 1
What Precision Endoscopy of America, Inc. makes
Precision Endoscopy of America, Inc. manufactures nozzle replacement kits designed for use with gastroscopes and colonoscopes. These kits provide disposable components intended to maintain and enhance the functionality of endoscopic equipment during procedures.
The company’s products fall under FDA Class II regulatory classification and are listed via the 510(k) pathway. These devices are intended for use within the United States, where they are subject to compliance with FDA requirements for endoscopic accessories.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Precision Endoscopy of America, Inc. have in the registry?
The registry currently lists 1 device for Precision Endoscopy of America, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Precision Endoscopy of America, Inc.'s devices?
Among its 1 most recently registered device, Precision Endoscopy of America, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Precision Endoscopy of America, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Precision Endoscopy of America, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Precision Endoscopy of America, Inc. in the registry?
The most recently registered devices listed for Precision Endoscopy of America, Inc. include GASTROSCOPE AND COLONOSCOPE NOZZLE REPLACEMENT KITS.