510(k) K932801 ยท DQX Wire, Guide, Catheter
CARDIMA SEEKER AND STUBBIE GUIDEWIRES
| Applicant | Cardima, Inc., Fremont CA, US |
| Decision | Substantially Equivalent, Sep 1, 1993 |
| Received | Jun 9, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K932801
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.