510(k) K903001 ยท HIT Tester, Color Vision
SLIMCATH (TM)
| Applicant | Gynopharma, Inc., Princeton NJ, US |
| Decision | Substantially Equivalent, Jun 25, 1991 |
| Received | Jul 9, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K903001
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.