510(k) K963716 ยท DXC Clamp, Vascular
MICS DEVICE SYSTEM
| Applicant | Percutaneous Technologies, Inc., Walnut CA, US |
| Decision | Substantially Equivalent, Apr 2, 1997 |
| Received | Sep 16, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K963716
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.