510(k) K800223 ยท IWE Monitor, Patient Position, Light-Beam
PATIENT POSITIONING SYSTEM 1D OR 2D
| Applicant | Laboratoire National D'Essais, Mchenry IL, US |
| Decision | Substantially Equivalent, Mar 3, 1980 |
| Received | Feb 4, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K800223
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.