510(k) K913940 ยท DRA Catheter, Steerable
RESPONSE(TM) STEERABLE CATHETER
| Applicant | Daig Corp., Minnetonka MN, US |
| Decision | Substantially Equivalent, Jan 26, 1993 |
| Received | Sep 3, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K913940
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.