Venowave, Inc.
CanadaFDA applicant, unverified
- Devices
- 1
What Venowave, Inc. makes
Venowave, Inc. manufactures venous access devices, specifically the VENOWAVE models VW5-6, VW5-10, VW5-20, and VW5-30, which are designed for peripheral intravenous catheterization and blood collection procedures.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) clearance process. The company is based in the United States.
Catalogue
Venowave Models VW5-6, VW5-10, VW5-20 And VW5-30 Ref K073028
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Venowave, Inc. have in the registry?
The registry currently lists 1 device for Venowave, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Venowave, Inc.'s devices?
Among its 1 most recently registered device, Venowave, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Venowave, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Venowave, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Venowave, Inc. in the registry?
The most recently registered devices listed for Venowave, Inc. include VENOWAVE MODELS VW5-6, VW5-10, VW5-20 AND VW5-30.