510(k) K961122 ยท FTD Lamp, Surgical
STRYKER KNIFELIGHT
| Applicant | Stryker Instruments, Kalamazoo MI, US |
| Decision | Substantially Equivalent, Aug 22, 1996 |
| Received | Mar 21, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K961122
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.