510(k) K973757 ยท MPA Endoilluminator
D.O.R.C. SOLUX LIGHT SOURCE
| Applicant | Dutch Ophthalmic USA, Inc., Kingston NH, US |
| Decision | Substantially Equivalent, Nov 7, 1997 |
| Received | Oct 2, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K973757
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.