510(k) K913013 ยท LKD Monitor, Carbon-Dioxide, Cutaneous
TCPO2 9260 MODULE - SYSTEM ATHENA
| Applicant | S & W Medico Teknik, Denmark, DK |
| Decision | Substantially Equivalent, May 3, 1994 |
| Received | Jul 8, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K913013
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.