510(k) K081823 ยท CCM Plethysmograph, Pressure
MASTERSCREEN PAED - BABY BODY
| Applicant | Viasys Healthcare GmbH, Hoechberg, DE |
| Decision | Substantially Equivalent, May 18, 2009 |
| Received | Jun 27, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K081823
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.