510(k) K980756 ยท LKD Monitor, Carbon-Dioxide, Cutaneous
COROMETRICS TRANSCUTANEOUS TCPO2/CO2 MODULE
| Applicant | Ge Medical Systems Information Technologies, Wallingford CT, US |
| Decision | Substantially Equivalent, Nov 5, 1998 |
| Received | Feb 27, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K980756
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.