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FDA 510(k) Application Details - K980350
Device Classification Name
Laparoscope, General & Plastic Surgery
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510(K) Number
K980350
Device Name
Laparoscope, General & Plastic Surgery
Applicant
CUDA PRODUCTS CO.
6000 POWERS AVE.
JACKSONVILLE, FL 32217 US
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Contact
KIM REED
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
01/28/1998
Decision Date
04/28/1998
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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