Velocimed, Inc.
United StatesFDA applicant, unverified
- Devices
- 6
What Velocimed, Inc. makes
Velocimed, Inc. manufactures medical devices including the Proxis system, the Venture wire control catheter, and the Premere delivery sheath. These products are designed for use in interventional procedures.
The company is based in the United States, and its portfolio consists of Class II medical devices. These products are listed in the FDA 510(k) regulatory registry.
Catalogue
Proxis System, Model Eps 101 Ref K042117
Regimes: 510(k) Registry: 510(k)Venture Wire Control Catheter Ref K040922
Regimes: 510(k) Registry: 510(k)Venture Wire Control Catheter, Model Wcc Ref K042910
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Proxis System Ref K052523
Regimes: 510(k) Registry: 510(k)Premere Delivery Sheath, Model Pds Ref K043084
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Velocimed, Inc. have in the registry?
The registry currently lists 6 devices for Velocimed, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Velocimed, Inc.'s devices?
Among its 6 most recently registered devices, Velocimed, Inc. has devices listed in FDA 510(k) (6 devices).
What risk classes do Velocimed, Inc.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Velocimed, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Velocimed, Inc. in the registry?
The most recently registered devices listed for Velocimed, Inc. include PROXIS SYSTEM, MODEL EPS 101, VENTURE WIRE CONTROL CATHETER, VENTURE WIRE CONTROL CATHETER, MODEL WCC and PROXIS FLOW-CONTROL DEVICE, MODELS EPS 101, IC 101.