D-R Medical Systems, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 3
Catalogue
Velex Woven External Velour Dacron Graft Ref K880040
510(k) 510(k)Velex Woven Dacron Low Porsity Vascular Graft Ref K880041
510(k) 510(k)Extended Package Dating On Velex Woven Grafts Ref K890597
510(k) 510(k)
Frequently asked questions
How many devices does D-R Medical Systems, Inc. have in the registry?
The registry currently lists 3 devices for D-R Medical Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list D-R Medical Systems, Inc.'s devices?
Among its 3 most recently registered devices, D-R Medical Systems, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do D-R Medical Systems, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for D-R Medical Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from D-R Medical Systems, Inc. in the registry?
The most recently registered devices listed for D-R Medical Systems, Inc. include VELEX WOVEN EXTERNAL VELOUR DACRON GRAFT, VELEX WOVEN DACRON LOW PORSITY VASCULAR GRAFT and EXTENDED PACKAGE DATING ON VELEX WOVEN GRAFTS.