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FDA 510(k) Application Details - K984310
Device Classification Name
Tubes, Gastrointestinal (And Accessories)
More FDA Info for this Device
510(K) Number
K984310
Device Name
Tubes, Gastrointestinal (And Accessories)
Applicant
MOSS TUBES, INC.
304 VERONA AVE.
ELIZABETH, NJ 07208 US
Other 510(k) Applications for this Company
Contact
HARRY A SCHLAKMAN
Other 510(k) Applications for this Contact
Regulation Number
876.5980
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Classification Product Code
KNT
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
12/02/1998
Decision Date
02/24/1999
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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