510(k) K811836 ยท KLK Monitor, Oxygen, Cutaneous, For Infant Not Under Gas Anesthesia
PO-200 BLOOD OXYGEN MONITOR
| Applicant | Sumitomo Electric Industries, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Jul 27, 1981 |
| Received | Jun 30, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K811836
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.