510(k) K121929 ยท FRZ Device, Patient Transfer, Powered
ZEPHYR 'X-SERIES PATIENT TRANSFER SLED
| Applicant | Diacor, Inc., West Valley City UT, US |
| Decision | Substantially Equivalent, Jan 17, 2013 |
| Received | Jul 2, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K121929
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.