Lifequest Medical, Inc.
Country not established
- Devices
- 1
What Lifequest Medical, Inc. makes
Lifequest Medical, Inc. manufactures the INTROPORT™ Catheter Model #1000 (ICT), a medical device designed for vascular access procedures.
The INTROPORT™ Catheter Model #1000 (ICT) is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Introport(Tm) Catheter Model #1000(Ict) Ref K946189
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lifequest Medical, Inc. have in the registry?
The registry currently lists 1 device for Lifequest Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lifequest Medical, Inc.'s devices?
Among its 1 most recently registered device, Lifequest Medical, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Lifequest Medical, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Lifequest Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Lifequest Medical, Inc. in the registry?
The most recently registered devices listed for Lifequest Medical, Inc. include INTROPORT(TM) CATHETER MODEL #1000(ICT).