510(k) K935760 ยท IWE Monitor, Patient Position, Light-Beam
TEC 2100 (MODEL MT-LPLGD)
| Applicant | Medtec, Inc., Orange City IA, US |
| Decision | Substantially Equivalent, Jan 25, 1994 |
| Received | Nov 26, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K935760
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.