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FDA 510(k) Application Details - K141359
Device Classification Name
Syringe, Piston
More FDA Info for this Device
510(K) Number
K141359
Device Name
Syringe, Piston
Applicant
JIANGYIN CAINA TECHNOLOGY CO., LTD
P.O. BOX 120-119
SHANGHAI 200120 CN
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Contact
Diana Hong
Other 510(k) Applications for this Contact
Regulation Number
880.5860
More FDA Info for this Regulation Number
Classification Product Code
FMF
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
05/23/2014
Decision Date
07/25/2014
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
HO - General Hospital
Review Advisory Committee
HO - General Hospital
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
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