510(k) K896609 ยท IZH System, X-Ray, Mammographic
CYTOGUIDE FOR USE W/THE PHILMEDISYST MAMMODIAG UC
| Applicant | Philips Medical Systems North America, Inc., Shelton CT, US |
| Decision | Substantially Equivalent, Jan 31, 1990 |
| Received | Aug 9, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896609
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.