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FDA 510(k) Application Details - K123806
Device Classification Name
System, Imaging, Pulsed Echo, Ultrasonic
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510(K) Number
K123806
Device Name
System, Imaging, Pulsed Echo, Ultrasonic
Applicant
ECHOSENS
990 WASHINGTON STREET, STE #204
DEDHAM, MA 02026 US
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Contact
ZVI LADIN, PH.D.
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Regulation Number
892.1560
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Classification Product Code
IYO
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More FDA Info for this Product Code
Date Received
12/10/2012
Decision Date
04/05/2013
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
RA - Radiology
Review Advisory Committee
RA - Radiology
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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