510(k) K914184 ยท KPW Device, Beam Limiting, X-Ray, Diagnostic
P2020-8-0 BEAM-LIMITING DEVICE
| Applicant | Precise Optics, Bay Shore NY, US |
| Decision | Substantially Equivalent, Nov 27, 1991 |
| Received | Sep 18, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K914184
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.