510(k) K952924 ยท GBM Catheter, Urethral
ADI CATHETER WITH VALVE
| Applicant | Asia Dynamics, Inc., Niles IL, US |
| Decision | Substantially Equivalent, Aug 18, 1995 |
| Received | Jun 26, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K952924
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.