510(k) K810153 ยท FLS Monitor, Apnea, Facility Use
VENTILATORY EFFORT MONITOR
| Applicant | Medicon, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Feb 9, 1981 |
| Received | Jan 21, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K810153
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.