510(k) K003505 ยท MOS Coil, Magnetic Resonance, Specialty
KFA-127 KNEE, FOOT AND ANKLE ARRAY
| Applicant | Mri Devices Corp., Waukesha WI, US |
| Decision | Substantially Equivalent, May 25, 2001 |
| Received | Nov 13, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K003505
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.