510(k) K910902 ยท IZL System, X-Ray, Mobile
VMX MOBILE X-RAY SYSTEM
| Applicant | GE Medical Systems, Milwaukee WI, US |
| Decision | Substantially Equivalent, Sep 9, 1991 |
| Received | Mar 5, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K910902
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Apr 10, 2013 | GE Healthcare, LLC VMX, VMX Plus Mobile Radiographic Unit with the following models:
45296139; 45296200; 45296350; 45296477; 45296964; 45297001; 45296966; 45297003; 2240169; 2240171; 2240172; 2240173.
Product Usage: Terminated |
IZL | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.