510(k) K023254 ยท GBM Catheter, Urethral
SPEEDICATH
| Applicant | Coloplast Corp., North Mankato MN, US |
| Decision | Substantially Equivalent, Jan 27, 2003 |
| Received | Sep 30, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K023254
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.