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FDA 510(k) Application Details - K101733
Device Classification Name
Laparoscope, General & Plastic Surgery
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510(K) Number
K101733
Device Name
Laparoscope, General & Plastic Surgery
Applicant
SAC, LLC DBA PINNACLE MEDICAL SURGICAL
P.O. BOX 782108
ORLANDO, FL 32878-2108 US
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DAVE STRAIN
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Regulation Number
876.1500
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Classification Product Code
GCJ
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More FDA Info for this Product Code
Date Received
06/21/2010
Decision Date
06/06/2011
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
GU - Gastroenterology & Urology
Review Advisory Committee
SU - General & Plastic Surgery
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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