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FDA 510(k) Application Details - K020956
Device Classification Name
Media,Coupling,Ultrasound
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510(K) Number
K020956
Device Name
Media,Coupling,Ultrasound
Applicant
MICROTEK MEDICAL, INC.
602 LEHMBERG RD.
COLUMBUS, MS 39702 US
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THOMAS BONNER
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Regulation Number
892.1570
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Classification Product Code
MUI
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More FDA Info for this Product Code
Date Received
03/25/2002
Decision Date
05/16/2002
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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