510(k) K881882 ยท IZH System, X-Ray, Mammographic
SENOGRAPHE 600T AND 600TS SENIX HF
| Applicant | General Electric Co., Milwaukee WI, US |
| Decision | Substantially Equivalent, May 25, 1988 |
| Received | May 4, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881882
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jul 20, 2004 | General Electric Med Systems Seneographe 600 Mammography X-Ray Systems (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.