510(k) K853757 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
MOLDTEC STIMULATOR
| Applicant | Moldtec, Inc., New Orleans LA, US |
| Decision | Substantially Equivalent, Feb 28, 1986 |
| Received | Sep 9, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K853757
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.