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FDA 510(k) Application Details - K030120
Device Classification Name
Catheter, Retention Type, Balloon
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510(K) Number
K030120
Device Name
Catheter, Retention Type, Balloon
Applicant
AMSINO INTERNATIONAL, INC.
4501 BRICKELL PRIVADO ST.
ONTARIO, CA 91761 US
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Contact
CHING CHING SEAH
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Regulation Number
876.5130
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Classification Product Code
EZL
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More FDA Info for this Product Code
Date Received
01/13/2003
Decision Date
10/29/2003
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
GU - Gastroenterology & Urology
Review Advisory Committee
GU - Gastroenterology & Urology
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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