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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Polymer Patient Examination Glove
510(k) Number K983729
Device Name POWDER-FREE NITRILE PATIENT EXAMINATION GLOVE
Applicant
Perusahaan Getah Asas Sdn. Bhd.
Lot 754, Jalan Haji Sirat
Selangor,  MY 41720
Applicant Contact BOB CHAN
Correspondent
Perusahaan Getah Asas Sdn. Bhd.
Lot 754, Jalan Haji Sirat
Selangor,  MY 41720
Correspondent Contact BOB CHAN
Regulation Number880.6250
Classification Product Code
LZA  
Date Received10/22/1998
Decision Date 12/11/1998
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Statement Statement
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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