510(k) K896384 ยท EQH Source, Carrier, Fiberoptic Light
FIBEROPTIC LIGHT SOURCE, FOI-1A
| Applicant | Jedmed Instrument Co., St. Louis MO, US |
| Decision | Substantially Equivalent, Jan 23, 1990 |
| Received | Nov 6, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896384
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.