510(k) K821936 ยท KLK Monitor, Oxygen, Cutaneous, For Infant Not Under Gas Anesthesia
CRITIKON OXYGEN MONITOR, MODEL 8030
| Applicant | Critikon Company, LLC, Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 16, 1982 |
| Received | Jun 29, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K821936
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.