FDA 510(k) Applications Submitted by NASIFF ASSOC., INC.

FDA 510(k) Number Submission Date Device Name Applicant
K960544 02/07/1996 CARDIO-CARD HOLTER ECG MANAGEMENT SYSTEM NASIFF ASSOC., INC.
K972795 07/28/1997 CARDIO-CARD MANAGEMENT SYSTEM II NASIFF ASSOC., INC.
K993616 10/26/1999 CARDIO-CARD INTERPRETATION SYSTEM I NASIFF ASSOC., INC.


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