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FDA 510(k) Application Details - K070026
Device Classification Name
Vinyl Patient Examination Glove
More FDA Info for this Device
510(K) Number
K070026
Device Name
Vinyl Patient Examination Glove
Applicant
SHIJIAZHUANG LIANHE SHUNDA PLASTIC PRODUCTS CO., L
3973 SCHAEFER AVE
CHINO, CA 91710 US
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Contact
KATHY LIU
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
01/03/2007
Decision Date
03/07/2007
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
HO - General Hospital
Review Advisory Committee
HO - General Hospital
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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