510(k) K030129 ยท DQK Computer, Diagnostic, Programmable
MODIFICATION TO ENSITE 3000 SYSTEM, MODEL EE3000
| Applicant | Endocardial Solutions, Inc., St. Paul MN, US |
| Decision | Unknown, Apr 22, 2003 |
| Received | Jan 14, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K030129
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.