510(k) K813347 ยท KLK Monitor, Oxygen, Cutaneous, For Infant Not Under Gas Anesthesia
CRITIKON TRANSCUTANEOUS GAS MONITORS
| Applicant | Critikon Company, LLC, Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 26, 1982 |
| Received | Nov 27, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K813347
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.