510(k) K915274 ยท FST Light, Surgical, Fiberoptic
METAL HALIDE LIGHT SOURCE MODEL LM 250
| Applicant | Pentax Precision Instrument Corp., Orangeburg NY, US |
| Decision | Substantially Equivalent, Jan 23, 1992 |
| Received | Nov 25, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K915274
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.