510(k) K900333 ยท LKD Monitor, Carbon-Dioxide, Cutaneous
E5280 COMBINED TRANSCUTANEOUS TCP02/TCPCO2 ELECT.
| Applicant | Radiometer America, Inc., Westlake OH, US |
| Decision | Substantially Equivalent, Apr 16, 1990 |
| Received | Jan 23, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900333
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.