510(k) K780765 ยท KOB Catheter, Suprapubic (And Accessories)
PERCUTANEOUS SURAPUBIC CATHETER
| Applicant | Vance Products, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Jul 17, 1978 |
| Received | May 5, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K780765
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.