510(k) K943851 ยท GBM Catheter, Urethral
ALL SILICONE INTERMITTENT CATHETER
| Applicant | Rochester Medical Corp., Stewartville MN, US |
| Decision | Substantially Equivalent, Jan 31, 1995 |
| Received | Aug 8, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K943851
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.