FDA 510(k) Applications Submitted by NORTH AMERICAN INSTRUMENT CORP.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K960801 | 02/27/1996 | SELECTOR ANGIOGRAPHIC CATHETER (VARIOUS MODELS) | NORTH AMERICAN INSTRUMENT CORP. |
| K960310 | 01/22/1996 | EPIC INTRODUCER SHEATH | NORTH AMERICAN INSTRUMENT CORP. |
| K955554 | 12/05/1995 | HEMO-VALVE | NORTH AMERICAN INSTRUMENT CORP. |
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