510(k) K873786 ยท FSY Light, Surgical, Ceiling Mounted
SMITH & NEPHEW DAYLIGHTER(TM)
| Applicant | Smith & Nephew, Inc., St. Louis MO, US |
| Decision | Substantially Equivalent, Oct 23, 1987 |
| Received | Sep 17, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K873786
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.