510(k) K901603 ยท KOB Catheter, Suprapubic (And Accessories)
MODIFIED PORGES SPEC 5* SUPRAPUBIC CATHETER
| Applicant | Bivona Medical Technologies, Gary IN, US |
| Decision | Substantially Equivalent, May 4, 1990 |
| Received | Mar 27, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K901603
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.