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Koven and Assoc., Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
8
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K922669MULTIDOP MODEL HD-2020 BI-DIRECTIONAL BLOOD FLOWJanuary 29, 1993
K920333SMARTDOP 20 BI-DIRECTIONAL BLOOD FLOW DETECTORJanuary 22, 1993
K915550MINI DOPPLER II ULTRASOUND BLOOD FLOW DETECTORDecember 10, 1992
K913595DS-240 AMBULATORY BLOOD PRESSURE MONITORING SYSTEMMarch 27, 1992
K912409MODEL HD-207 BIDIRECTIONAL VELOCITY METERDecember 23, 1991
K903026ES-1000SP II SMART DOPFebruary 26, 1991
K894892HD-2200 PNEUMO-DOP VASCULAR TESTING SYSTEMOctober 27, 1989
K892707DVM-4200 BLOOD FLOWMETERJuly 28, 1989