Lifequest Endoscopic Technologies, Inc.
Country not established
- Devices
- 1
What Lifequest Endoscopic Technologies, Inc. makes
Lifequest Endoscopic Technologies, Inc. manufactures the LQUET Cannula/Trocar System, a device used in endoscopic procedures to facilitate access and insertion of instruments into the body.
The company’s portfolio is regulated under FDA Class II devices and is listed via the 510(k) clearance pathway. The manufacturer is based in the United States.
Catalogue
Lquet Cannula/Trocar System Ref K974139
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lifequest Endoscopic Technologies, Inc. have in the registry?
The registry currently lists 1 device for Lifequest Endoscopic Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lifequest Endoscopic Technologies, Inc.'s devices?
Among its 1 most recently registered device, Lifequest Endoscopic Technologies, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Lifequest Endoscopic Technologies, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Lifequest Endoscopic Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Lifequest Endoscopic Technologies, Inc. in the registry?
The most recently registered devices listed for Lifequest Endoscopic Technologies, Inc. include LQUET CANNULA/TROCAR SYSTEM.