Veinrx, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: 510(k) Registry: 510(k)
Varicath Peripheral Infusion Catheter Ref K073400
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Veinrx, Inc. have in the registry?
The registry currently lists 2 devices for Veinrx, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Veinrx, Inc.'s devices?
Among its 2 most recently registered devices, Veinrx, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Veinrx, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Veinrx, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Veinrx, Inc. in the registry?
The most recently registered devices listed for Veinrx, Inc. include INFUSIONCATH PERIPHERAL INFUSION CATHETER, MODELS VF0012, VF0016, VF0024, VF0028, VF0032, VF0036, VF0040, VF0044 and VARICATH PERIPHERAL INFUSION CATHETER.