510(k) K842609 ยท FCW Light Source, Fiberoptic, Routine
R.L. MEDICAL TWIN LIGHT SOURCE
| Applicant | Tridak Division of Indicon, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 9, 1984 |
| Received | Jul 5, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K842609
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.