510(k) K883069 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
MINIMON 7134B PATIENT MONITOR
| Applicant | Kontron Instruments, Inc., Everett MA, US |
| Decision | Substantially Equivalent, Jan 17, 1989 |
| Received | Jul 20, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883069
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.