510(k) K872489 ยท IWE Monitor, Patient Position, Light-Beam
CENTRALITE
| Applicant | Diacor, Inc., Salt Lake City UT, US |
| Decision | Substantially Equivalent, Jul 15, 1987 |
| Received | Jun 23, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K872489
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.