510(k) K983456 ยท MTD Catheter, Intracardiac Mapping, High-Density Array
ENSITE 3000 SYSTEM
| Applicant | Endocardial Solutions, Inc., St. Paul MN, US |
| Decision | Unknown, Apr 21, 1999 |
| Received | Sep 30, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K983456
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.