Bowman/Vector, Inc.
Country not established
- Devices
- 1
What Bowman/Vector, Inc. makes
Bowman/Vector, Inc. manufactures an interjector blood collection device, designed for automated or semi-automated blood sampling and processing in clinical or laboratory settings.
The company’s portfolio is regulated under FDA Class II devices, with products listed via the 510(k) clearance pathway. The manufacturer is based in the United States.
Catalogue
Interjector Blood Collection Device Ref K901756
510(k) 510(k)
Frequently asked questions
How many devices does Bowman/Vector, Inc. have in the registry?
The registry currently lists 1 device for Bowman/Vector, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bowman/Vector, Inc.'s devices?
Among its 1 most recently registered device, Bowman/Vector, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Bowman/Vector, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Bowman/Vector, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bowman/Vector, Inc. in the registry?
The most recently registered devices listed for Bowman/Vector, Inc. include INTERJECTOR BLOOD COLLECTION DEVICE.