510(k) K885126 ยท KQA Device, Beam Limiting, X-Ray, Therapeutic
PHILIPS RT250 COLLIMATOR (PK8050)
| Applicant | Perkins Mfg. Co., Dallas TX, US |
| Decision | Substantially Equivalent, Jun 1, 1989 |
| Received | Dec 12, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K885126
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.