FDA 510(k) Applications Submitted by MARY MEAGHER RUBIN

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.
K951722 04/14/1995 PERCEPTOR COMPENSATOR MORSE MANIFOLD NAMIC
K955554 12/05/1995 HEMO-VALVE NORTH AMERICAN INSTRUMENT CORP.
K953676 08/07/1995 BREEZE DIGITAL INFLATION DEVICE NAMIC


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