510(k) K831752 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
BIOCHECK PEC-108 PROGRAM-PULSE MONITOR
| Applicant | Biotechnology, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Sep 29, 1983 |
| Received | Jun 1, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K831752
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.