FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

ECHOFLOW DOPPLER BLOOD VELOCITY METER

K Number: K990642 · Decision Sep 16, 1999
Classifications
1
FEI Numbers
16
Registration Numbers
16
Same Product Code
71
Applicant Total
6
Review Days
202

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Basic Information

Device Name
ECHOFLOW DOPPLER BLOOD VELOCITY METER
K Number
K990642
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2880
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Echocath, Inc.
Date Received
February 26, 1999
Decision Date
September 16, 1999
Product Code
JOP
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JOP Transducer, Ultrasonic

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Other Clearances by Echocath, Inc.

K Number Device Name
K010482 ECHOFLOW PORTABLE DOPPLER BLOOD FLOW MEASUREMENT SYSTEM; MODEL PEF-1
K932436 ECHOMARK INTRAUTERINE GUIDING CATHETER
K933417 ECHOMARK(R) ELECTROPHYSIOLOGY CATHETER
K926351 COLORMARK(TM) VISUALIZATION SYSTEM
K922787 ECHOMARK GUIDEWIRE WITH ULTRASONIC LOCALIZATION