510(k) K902381 ยท CAP Monitor, Airway Pressure (Includes Gauge And/Or Alarm)
PENLON BREATHING SYSTEM PRESSURE MONITOR
| Applicant | Penlon, Inc., Newtown PA, US |
| Decision | Substantially Equivalent, Aug 17, 1990 |
| Received | May 30, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K902381
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.