510(k) K923141 ยท ITY Assembly, Tube Housing, X-Ray, Diagnostic
PHILIPS PRE-FILTER OPTION
| Applicant | Philips Medical Systems, Inc., 5680 Da Best, NL |
| Decision | Substantially Equivalent, Jan 21, 1993 |
| Received | Jun 29, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K923141
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.