510(k) K122050 ยท LIX Aid, Cardiopulmonary Resuscitation
CPRMETER CPR FEEDBACK DEVICE
| Applicant | Laerdal Medical A/S, West Lafayette IN, US |
| Decision | Substantially Equivalent, Oct 22, 2012 |
| Received | Jul 12, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K122050
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.