510(k) K951603 ยท DQY Catheter, Percutaneous
CARDIMA, INC. FORERUNNER
| Applicant | Cardima, Inc., Fremont CA, US |
| Decision | Substantially Equivalent, Oct 5, 1995 |
| Received | Apr 7, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K951603
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.