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FDA 510(k) Application Details - K962329
Device Classification Name
Syringe, Piston
More FDA Info for this Device
510(K) Number
K962329
Device Name
Syringe, Piston
Applicant
GLOBAL MEDICAL PRODS, INC.
244 MAIN ST. SOUTH
P.O. 505
WOODBURY, CT 06798-0505 US
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Contact
PETER CLARK
Other 510(k) Applications for this Contact
Regulation Number
880.5860
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Classification Product Code
FMF
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More FDA Info for this Product Code
Date Received
06/17/1996
Decision Date
09/12/1996
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
HO - General Hospital
Review Advisory Committee
HO - General Hospital
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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