510(k) K932800 ยท KRA Catheter, Continuous Flush
CARDIMA TRACKER(R) INFUSION CATHETER
| Applicant | Cardima, Inc., Fremont CA, US |
| Decision | Substantially Equivalent, Dec 21, 1993 |
| Received | Jun 9, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K932800
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.