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FDA 510(k) Applications Submitted by MULTISAFE SDN BHD
FDA 510(k) Number
Submission Date
Device Name
Applicant
K062526
08/28/2006
BLUE POWDERED LATEX EXAMINATION GLOVES, NON-STERILE
MULTISAFE SDN BHD
K062527
08/28/2006
BLUE POWDER FREE LATEX EXAMINATION GLOVES, NON-STERILE
MULTISAFE SDN BHD
K011293
04/30/2001
POWDER FREE POLYMER COATED LATEX MEDICAL EXAMINATION GLOVES, NON-STERILE W/ PROTEIN CONTENT LABELING CLAIM 50 MCG OR LES
MULTISAFE SDN BHD
K001497
05/15/2000
MULTISAFE-POWDERED NITRILE GLOVES, NON-STERILE (BLUE)
MULTISAFE SDN BHD
K000999
03/28/2000
MULTISAFE POWDER-FREE PATIENT LATEX EXAMINATION GLOVES WITH PROTEIN CONTENT LABELING CLAIM (50 MICROGRAMS OR LESS)
MULTISAFE SDN BHD
K001619
05/25/2000
MULTISAFE POWDER FREE NITRILE GLOVES, NON STERILE (BLUE)
MULTISAFE SDN BHD
K993811
11/10/1999
MULTISAFE POWDERED LATEX EXAMINATION GLOVES, NONSTERILE
MULTISAFE SDN BHD
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