510(k) K072061 ยท JEH Plethysmograph, Volume
MASTERSCREEN PFT, MASTERSCREEN PFT CT, MASTERSCREEN PFT BODY
| Applicant | Viasys Healthcare GmbH, Yorba Linda CA, US |
| Decision | Substantially Equivalent, Apr 22, 2008 |
| Received | Jul 27, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072061
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.