510(k) K913733 ยท GBW Catheter, Peritoneal
STERILE CHEST TUBE
| Applicant | Vascular Products, Inc., Palm Florida FL, US |
| Decision | Substantially Equivalent, Oct 8, 1991 |
| Received | Aug 20, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K913733
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.