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FDA 510(k) Application Details - K152692
Device Classification Name
Vinyl Patient Examination Glove
More FDA Info for this Device
510(K) Number
K152692
Device Name
Vinyl Patient Examination Glove
Applicant
Supermax Plastic Products Co., Ltd
314 Dragon River East Road
Shijiazhuang City 050000 CN
Other 510(k) Applications for this Company
Contact
Wu Zhigang
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
09/21/2015
Decision Date
12/21/2015
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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