510(k) K860951 ยท KLK Monitor, Oxygen, Cutaneous, For Infant Not Under Gas Anesthesia
KONTRON CUTANEOUS PO2 MONITOR 820
| Applicant | Kontron Instruments, Inc., Everett MA, US |
| Decision | Substantially Equivalent, Apr 9, 1986 |
| Received | Mar 12, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K860951
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.