510(k) K950112 ยท IWE Monitor, Patient Position, Light-Beam
CENTRALITE(R)-DLL SERIES
| Applicant | Diacor, Inc., Salt Lake City UT, US |
| Decision | Substantially Equivalent, Aug 16, 1995 |
| Received | Jan 11, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K950112
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.