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FDA 510(k) Application Details - K091422
Device Classification Name
Vinyl Patient Examination Glove
More FDA Info for this Device
510(K) Number
K091422
Device Name
Vinyl Patient Examination Glove
Applicant
NOVAPRO CO., LTD.
NO. 21 QINGTIAN ROAD
LOT 4
ZIBO, SHANDONG 255414 CN
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Contact
ZHENZHONG CHENG
Other 510(k) Applications for this Contact
Regulation Number
880.6250
More FDA Info for this Regulation Number
Classification Product Code
LYZ
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More FDA Info for this Product Code
Date Received
05/13/2009
Decision Date
07/30/2009
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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