510(k) K923619 ยท IWE Monitor, Patient Position, Light-Beam
ACCULITE SSL
| Applicant | Medical Alignment Systems, Salt Lake City UT, US |
| Decision | Substantially Equivalent, Nov 16, 1992 |
| Received | Jul 21, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K923619
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.