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FDA 510(k) Application Details - K070242
Device Classification Name
Catheter, Ultrasound, Intravascular
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510(K) Number
K070242
Device Name
Catheter, Ultrasound, Intravascular
Applicant
BIOSENSE WEBSTER, INC.
3333 DIAMOND CANYON RD.
DIAMOND BAR, CA 91765 US
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Contact
NEELU MEDHEKAR
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Regulation Number
870.1200
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Classification Product Code
OBJ
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More FDA Info for this Product Code
Date Received
02/09/2007
Decision Date
05/15/2007
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
CV - Cardiovascular
Review Advisory Committee
CV - Cardiovascular
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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