510(k) K903966 ยท DTC Analyzer, Pacemaker Generator Function
EXTERNAL PACEMAKER ANALYZER MODEL PMA-1
| Applicant | Bio-Tek Instruments, Inc., Winooski VT, US |
| Decision | Substantially Equivalent, Jun 19, 1991 |
| Received | Aug 28, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K903966
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.