510(k) K853318 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
PATIENT MONITOR PB240
| Applicant | Puritan Bennett Corp., Overland Park KS, US |
| Decision | Substantially Equivalent, Mar 11, 1986 |
| Received | Aug 7, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K853318
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.