510(k) K990960 ยท LKD Monitor, Carbon-Dioxide, Cutaneous
PERIMED TRANSCUTANEOUS PO2 AND PCO2 MONITOR (PF5040)
| Applicant | Perimed, Inc., Laurel MD, US |
| Decision | Substantially Equivalent, Sep 23, 1999 |
| Received | Mar 22, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K990960
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.