510(k) K915773 ยท DQA Oximeter
P-300 CAPNOGRAPH AND PULSE OXIMETER
| Applicant | Pryon Corp., Menomonee Falls WI, US |
| Decision | Substantially Equivalent, Jun 24, 1992 |
| Received | Dec 24, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K915773
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.