510(k) K951246 ยท FLS Monitor, Apnea, Facility Use
PROPAQ ENCORE 200 SERIES MONITOR WITH NEONATAL MODE AND IMPEDANCE PNEUMOGRAPHY OPTIONS
| Applicant | Protocol Systems, Inc., Beaverton OR, US |
| Decision | Substantially Equivalent - Subject to Tracking Reg., Feb 2, 1996 |
| Received | Mar 20, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K951246
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.