510(k) K864801 ยท GCT Light Source, Endoscope, Xenon Arc
THE KEYMED HI-LIGHT 250 LIGHT SOURCE
| Applicant | Keymed, Inc., Essex Ss2 5qh England, GB |
| Decision | Substantially Equivalent, Dec 24, 1986 |
| Received | Dec 9, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K864801
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.