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Echocath, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K010482ECHOFLOW PORTABLE DOPPLER BLOOD FLOW MEASUREMENT SYSTEM; MODEL PEF-1March 20, 2001
K990642ECHOFLOW DOPPLER BLOOD VELOCITY METERSeptember 16, 1999
K932436ECHOMARK INTRAUTERINE GUIDING CATHETERNovember 16, 1995
K933417ECHOMARK(R) ELECTROPHYSIOLOGY CATHETERMay 4, 1995
K926351COLORMARK(TM) VISUALIZATION SYSTEMSeptember 16, 1993
K922787ECHOMARK GUIDEWIRE WITH ULTRASONIC LOCALIZATIONJanuary 6, 1993