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FDA 510(k) Application Details - K163017
Device Classification Name
Patient Examination Glove, Specialty
More FDA Info for this Device
510(K) Number
K163017
Device Name
Patient Examination Glove, Specialty
Applicant
GMP MEDICARE SDN BHD
LOT/PT64593, JLN DAHLIA/KU8, KAW PERINDUSTRIAN MERU TIMUR
KLANG 41050 MY
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EVA VINONI BT MUSTAFA
Other 510(k) Applications for this Contact
Regulation Number
880.6250
More FDA Info for this Regulation Number
Classification Product Code
LZC
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
10/28/2016
Decision Date
03/22/2017
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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