510(k) K012362 ยท GDW Staple, Implantable
MODIFICATION TO VASCULAR CLOSURE DEVICE
| Applicant | Std Mfg., Inc., Stoughton MA, US |
| Decision | Substantially Equivalent, Aug 23, 2001 |
| Received | Jul 25, 2001 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K012362
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.