510(k) K953250 ยท IZH System, X-Ray, Mammographic
SENOGRAPHE PEARL AND SENOGRAPHE SAPPHIRE
| Applicant | GE Medical Systems, Milwaukee WI, US |
| Decision | Substantially Equivalent, Jan 26, 1996 |
| Received | Jul 12, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K953250
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jul 20, 2004 | General Electric Med Systems Seneographe 700T Mammography X-Ray Systems Terminated |
IZH | None listed |
| Jul 20, 2004 | General Electric Med Systems Seneographe 800T Mammography X-Ray Systems Terminated |
IZH | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.