Vaporflow Technology, Inc.
Country not established
- Devices
- 1
What Vaporflow Technology, Inc. makes
Vaporflow Technology, Inc. manufactures the Lundy Vaporizer System, a medical device designed for vaporizing fluids in surgical or procedural settings to reduce smoke and airborne contaminants.
The Lundy Vaporizer System is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Lundy Vaporizer System Ref K884090
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Vaporflow Technology, Inc. have in the registry?
The registry currently lists 1 device for Vaporflow Technology, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vaporflow Technology, Inc.'s devices?
Among its 1 most recently registered device, Vaporflow Technology, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Vaporflow Technology, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Vaporflow Technology, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vaporflow Technology, Inc. in the registry?
The most recently registered devices listed for Vaporflow Technology, Inc. include LUNDY VAPORIZER SYSTEM.