510(k) K092324 ยท DQA Oximeter
SPIROPRO
| Applicant | Viasys Healthcare GmbH, Hoechberg, DE |
| Decision | Substantially Equivalent, Sep 3, 2009 |
| Received | Aug 4, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K092324
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.