510(k) K801254 ยท CAP Monitor, Airway Pressure (Includes Gauge And/Or Alarm)
PENLON I.D.P. PRESSSURE FAILURE ALARM
| Applicant | Penlon, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Jun 9, 1980 |
| Received | May 28, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K801254
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.