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FDA 510(k) Application Details - K002542
Device Classification Name
Laparoscope, General & Plastic Surgery
More FDA Info for this Device
510(K) Number
K002542
Device Name
Laparoscope, General & Plastic Surgery
Applicant
GENICON, LC
573 WATERSCAPE WAY
ORLANDO, FL 32828 US
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Contact
GARY HABERLAND
Other 510(k) Applications for this Contact
Regulation Number
876.1500
More FDA Info for this Regulation Number
Classification Product Code
GCJ
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More FDA Info for this Product Code
Date Received
08/16/2000
Decision Date
10/23/2000
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
GU - Gastroenterology & Urology
Review Advisory Committee
SU - General & Plastic Surgery
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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