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FDA 510(k) Application Details - K000652
Device Classification Name
Latex Patient Examination Glove
More FDA Info for this Device
510(K) Number
K000652
Device Name
Latex Patient Examination Glove
Applicant
BETELCARE SDN BHD
71/2 MILES, OFF JALAN KAPAR
KAPAR
SELANGOR DARUL EHSAN 42200 MY
Other 510(k) Applications for this Company
Contact
KENG BENG SIAH
Other 510(k) Applications for this Contact
Regulation Number
880.6250
More FDA Info for this Regulation Number
Classification Product Code
LYY
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
02/28/2000
Decision Date
04/10/2000
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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