510(k) K033151 ยท MOS Coil, Magnetic Resonance, Specialty
KFA-12 KNEE, FOOT, AND ANKLE ARRAY COIL
| Applicant | Mri Devices Corp., Waukesha WI, US |
| Decision | Substantially Equivalent, Oct 10, 2003 |
| Received | Sep 30, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K033151
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.