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FDA 510(k) Application Details - K172931
Device Classification Name
System, Imaging, Pulsed Echo, Ultrasonic
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510(K) Number
K172931
Device Name
System, Imaging, Pulsed Echo, Ultrasonic
Applicant
Advanced Instrumentations, Inc.
6800 NW 77th Ct
Miami, FL 33166 US
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Contact
Jorge Millan
Other 510(k) Applications for this Contact
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
09/25/2017
Decision Date
12/01/2017
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
RA - Radiology
Review Advisory Committee
RA - Radiology
Statement / Summary / Purged Status
Summary
Type
Abbreviated
Reviewed By Third Party
N
Expedited Review
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