510(k) K961361 ยท GBM Catheter, Urethral
ASTA-CATH
| Applicant | A+ Products, West Newton MA, US |
| Decision | Substantially Equivalent, Oct 31, 1996 |
| Received | Apr 9, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K961361
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.