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FDA 510(k) Application Details - K181791
Device Classification Name
Laparoscope, General & Plastic Surgery
More FDA Info for this Device
510(K) Number
K181791
Device Name
Laparoscope, General & Plastic Surgery
Applicant
Genicon, Inc
6869 Stapoint Court
Suite 114
Winter Park, FL 32792 US
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Contact
Katlyn Kachman
Other 510(k) Applications for this Contact
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
07/05/2018
Decision Date
08/21/2018
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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