510(k) K864919 ยท KPK Marker, Ostia, Aorto-Saphenous Vein
SCANLAN (TM) VEIN/GRAFT HOLDER
| Applicant | Scanlan Intl., Inc., Saint Paul MN, US |
| Decision | Substantially Equivalent, Jan 12, 1987 |
| Received | Dec 16, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K864919
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.