510(k) K935157 ยท KPX Changer, Radiographic Film/Cassette
ARTICULATED, LAPAROSCOPIC, AND SIDE-VIEWING T-PROBES
| Applicant | Regulatory Consultants TO the Medical Device Indus, Sandy UT, US |
| Decision | Substantially Equivalent, Aug 9, 1994 |
| Received | Oct 28, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K935157
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.