510(k) K001303 ยท MOS Coil, Magnetic Resonance, Specialty
BREAST IMMOBILIZATION DEVICE MR-BY 160
| Applicant | Mri Devices Corp., Waukesha WI, US |
| Decision | Substantially Equivalent, Jun 20, 2000 |
| Received | Apr 24, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K001303
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.