510(k) K894738 ยท DWS Instruments, Surgical, Cardiovascular
MODEL 6888 LEAD TUNNELER
| Applicant | Cardiac Pacemakers, Inc., St. Paul MN, US |
| Decision | Substantially Equivalent, Sep 13, 1989 |
| Received | Jul 27, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K894738
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.