510(k) K924605 ยท LNH System, Nuclear Magnetic Resonance Imaging
MAGNETIC RESONANCE DIAGNOSTIC ACCESSORY
| Applicant | General Electric Co., Milwaukee WI, US |
| Decision | Substantially Equivalent, May 21, 1993 |
| Received | Sep 11, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K924605
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.