FDA 510(k) Applications Submitted by MICOR, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K991879 | 06/02/1999 | SPRING-WOUND EPIDURAL CATHETER | MICOR, INC. |
| K001717 | 06/05/2000 | MICOR CONDUCTION CATHETER | MICOR, INC. |
| K001940 | 06/26/2000 | MICOR ANESTHESIA CONDUCTION KIT | MICOR, INC. |
| K003966 | 12/22/2000 | WUNDCATH CONDUCTION CATHETER | MICOR, INC. |
| K031600 | 05/21/2003 | CONDUCTION CATHETER | MICOR, INC. |
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