FDA 510(k) Applications Submitted by NALTIAC MEDICAL, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K961180 | 03/26/1996 | NMI ANTEGRAD CARDIOPLEGIA CANNULA | NALTIAC MEDICAL, INC. |
| K961181 | 03/26/1996 | NMI VEIN GRAFT PERFUSION SET | NALTIAC MEDICAL, INC. |
| K961717 | 05/02/1996 | NMI RETROGRADE CARDIOPLEGIA CANNULA-RCCS | NALTIAC MEDICAL, INC. |
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