510(k) K884930 ยท IZZ Table, Radiographic, Non-Tilting, Powered
COMPAX MODEL 40, 400, 400T
| Applicant | General Electric Co., Milwaukee WI, US |
| Decision | Substantially Equivalent, Dec 22, 1988 |
| Received | Nov 25, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884930
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Nov 25, 2009 | GE Medical Systems, LLC GE Medical Systems, COMPAX 40E X-ray Systems, Models; 2208203, 2208205, 2244282, 2244284, 2225863, 2225864 , 2225865, 2225870, 2225881, and 2225882.
Intended to be used for general purpose radio Terminated |
IZZ | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.