510(k) K891481 ยท LKD Monitor, Carbon-Dioxide, Cutaneous
SIEMENS SIRECUST TRANSCUTANEOUS CARBON DIOXIDE
| Applicant | Siemens Medical Electronics, Danvers MA, US |
| Decision | Substantially Equivalent, Sep 29, 1989 |
| Received | Mar 17, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K891481
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.