Ultravac, Inc.
Country not established
- Devices
- 1
What Ultravac, Inc. makes
Ultravac, Inc. manufactures the Series 3 General Suction System, a medical-grade suction device designed for clinical use to remove fluids and debris from patient airways or surgical sites.
The Series 3 General Suction System is classified as a Class II device under FDA regulations and is authorised via the 510(k) clearance process. The company is based in the United States.
Catalogue
Series 3 General Suction System Ref K891129
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ultravac, Inc. have in the registry?
The registry currently lists 1 device for Ultravac, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ultravac, Inc.'s devices?
Among its 1 most recently registered device, Ultravac, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Ultravac, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Ultravac, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ultravac, Inc. in the registry?
The most recently registered devices listed for Ultravac, Inc. include SERIES 3 GENERAL SUCTION SYSTEM.