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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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