510(k) K131253 ยท LKD Monitor, Carbon-Dioxide, Cutaneous
PERIFLUX 6000
| Applicant | Perimed AB, Jarfalla, SE |
| Decision | Substantially Equivalent, Oct 22, 2013 |
| Received | May 2, 2013 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K131253
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.