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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Latex Patient Examination Glove
510(k) Number K933759
Device Name RUBBERCARE LOPRO PATIENT EXAMINATION GLOVES, POWDERED
Applicant
Perusahaan Pelindung Getah (M) Sdn Bhd
Empat, Senawang Industrial
Estate, 70450 Seremban, Negeri
Sembilan Darul Khusus Malaysia,  ML
Applicant Contact YEW NIENG CHOON
Correspondent
Perusahaan Pelindung Getah (M) Sdn Bhd
Empat, Senawang Industrial
Estate, 70450 Seremban, Negeri
Sembilan Darul Khusus Malaysia,  ML
Correspondent Contact YEW NIENG CHOON
Regulation Number880.6250
Classification Product Code
LYY  
Date Received07/21/1993
Decision Date 03/21/1994
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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