510(k) K950293 ยท IWE Monitor, Patient Position, Light-Beam
TEC-2110 GREEN LASER MODEL MT-HNG
| Applicant | Medtec, Inc., Orange City IA, US |
| Decision | Substantially Equivalent, Aug 18, 1995 |
| Received | Jan 25, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K950293
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.