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FDA 510(k) Application Details - K033693
Device Classification Name
Vinyl Patient Examination Glove
More FDA Info for this Device
510(K) Number
K033693
Device Name
Vinyl Patient Examination Glove
Applicant
SHEN WEI (USA), INC.
2845 WHIPPLE RD.
UNION CITY, CA 94587 US
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Contact
CYNTHIA LIU
Other 510(k) Applications for this Contact
Regulation Number
880.6250
More FDA Info for this Regulation Number
Classification Product Code
LYZ
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
11/24/2003
Decision Date
01/16/2004
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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