510(k) K913418 ยท IZH System, X-Ray, Mammographic
SENOGRAPHE DMR/SMR/DM
| Applicant | General Electric Co., Milwaukee WI, US |
| Decision | Substantially Equivalent, Jan 6, 1992 |
| Received | Jul 31, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K913418
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jul 20, 2004 | General Electric Med Systems Seneographe DMR Mammography X-Ray System (all versions) Terminated |
IZH | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.