510(k) K140588 ยท FXY Hood, Surgical
FLYTE HYBRID HOOD, FLYTE HYBRID HOOD WITH PEELAWAY LENS
| Applicant | Stryker Corporation, Kalamazoo MI, US |
| Decision | Substantially Equivalent, Jun 26, 2014 |
| Received | Mar 7, 2014 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K140588
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.