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FDA 510(k) Application Details - K160393
Device Classification Name
Laparoscope, General & Plastic Surgery
More FDA Info for this Device
510(K) Number
K160393
Device Name
Laparoscope, General & Plastic Surgery
Applicant
AESCULAP, INC.
3773 CORPORATE PARKWAY
Center Valley, PA 18034 US
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Contact
Jessica Stigliano
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
02/11/2016
Decision Date
05/26/2016
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
GU - Gastroenterology & Urology
Review Advisory Committee
SU - General & Plastic Surgery
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
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