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FDA 510(k) Application Details - K991918
Device Classification Name
Tubes, Gastrointestinal (And Accessories)
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510(K) Number
K991918
Device Name
Tubes, Gastrointestinal (And Accessories)
Applicant
VYGON CORP.
1129 BLOOMFIELD AVE.
WEST CALDWELL, NJ 07006 US
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Contact
ROBERT SCHIFF
Other 510(k) Applications for this Contact
Regulation Number
876.5980
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Classification Product Code
KNT
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More FDA Info for this Product Code
Date Received
06/07/1999
Decision Date
10/29/1999
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
GU - Gastroenterology & Urology
Review Advisory Committee
GU - Gastroenterology & Urology
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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