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FDA 510(k) Application Details - K961521
Device Classification Name
Vinyl Patient Examination Glove
More FDA Info for this Device
510(K) Number
K961521
Device Name
Vinyl Patient Examination Glove
Applicant
SHANGHAI PT PLASTICS ENTERPRISE COMPANY, LTD.
NO. 268, YUSHU ROAD
CANGQIAO TOWNSHIP
SONGJIANG COUNTY SHANGHAI CN
Other 510(k) Applications for this Company
Contact
PETER WANG
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
04/22/1996
Decision Date
01/30/1997
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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