Vascular Products, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Vascular Biopsy Forceps Ref K910840
Regimes: 510(k) Registry: 510(k)Sterile Chest Tube Ref K913733
Regimes: 510(k) Registry: 510(k)Implantable Pacing Lead, Tined #3262 & Ref K823447
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Vascular Products, Inc. have in the registry?
The registry currently lists 3 devices for Vascular Products, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vascular Products, Inc.'s devices?
Among its 3 most recently registered devices, Vascular Products, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Vascular Products, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Vascular Products, Inc.'s devices are Class I, Class II and Class III. Each device page shows its own class and authorisation.
What are the newest devices from Vascular Products, Inc. in the registry?
The most recently registered devices listed for Vascular Products, Inc. include VASCULAR BIOPSY FORCEPS, STERILE CHEST TUBE and IMPLANTABLE PACING LEAD, TINED #3262 &.