510(k) K033235 ยท MOS Coil, Magnetic Resonance, Specialty
GEMINI III HYBRID TX/RX 4 CHANNEL HEAD COIL
| Applicant | Usa Instruments, Inc., Aurora OH, US |
| Decision | Substantially Equivalent, Dec 17, 2003 |
| Received | Oct 6, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K033235
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.