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FDA 510(k) Applications Submitted by ECHOCATH, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K010482
02/20/2001
ECHOFLOW PORTABLE DOPPLER BLOOD FLOW MEASUREMENT SYSTEM; MODEL PEF-1
ECHOCATH, INC.
K990642
02/26/1999
ECHOFLOW DOPPLER BLOOD VELOCITY METER
ECHOCATH, INC.
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