510(k) K955236 ยท IWE Monitor, Patient Position, Light-Beam
GREEN TEC-2100
| Applicant | Medtec, Inc., Orange City IA, US |
| Decision | Substantially Equivalent, May 24, 1996 |
| Received | Nov 14, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K955236
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.