510(k) K072808 ยท GBM Catheter, Urethral
SPEEDICATH COMPACT
| Applicant | Coloplast Corp., Minneapolis MN, US |
| Decision | Substantially Equivalent, Nov 9, 2007 |
| Received | Oct 1, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072808
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.