510(k) K911888 ยท IZP Programmer, Changer, Film/Cassette, Radiographic
PHILIPS ANGIOPRO
| Applicant | Philips Medical Systems North America, Inc., Shelton CT, US |
| Decision | Substantially Equivalent, Oct 15, 1991 |
| Received | Apr 29, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K911888
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.