510(k) K801799 ยท LDF Electrode, Pacemaker, Temporary
ATRIAL/VENTRICULAR SEQENTIAL #080-20000
| Applicant | Medical Testing System, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 2, 1981 |
| Received | Jul 29, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K801799
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.