510(k) K883664 ยท IYB Tube Mount, X-Ray, Diagnostic
LUM VASCULAR PROCEDURE SYSTEM #B5200A
| Applicant | General Electric Co., Milwaukee WI, US |
| Decision | Substantially Equivalent, Nov 7, 1988 |
| Received | Aug 26, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883664
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.