510(k) K871149 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
DRM 2300 PLETHYSMOGRAPHIC CARDIOTACHOMETER
| Applicant | Iontec Corp., Hammond LA, US |
| Decision | Substantially Equivalent, Jun 5, 1987 |
| Received | Mar 23, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K871149
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.