510(k) K872443 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
COMPANION 50 REGULATOR/FLOWMETER
| Applicant | Puritan Bennett Corp., Overland Park KS, US |
| Decision | Substantially Equivalent, Jul 21, 1987 |
| Received | Jun 23, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K872443
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.