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FDA 510(k) Applications Submitted by FLEXITECH SDN. BHD.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K990499
02/17/1999
PREPOWDERED NITRILE EXAMINATION GLOVES
FLEXITECH SDN. BHD.
K990502
02/17/1999
PREPOWDERED LATEX EXAMINATION GLOVES WITH PROTEIN CONTENT LABELING CLAIM (100 MICROGRAMS OR LESS)
FLEXITECH SDN. BHD.
K990495
02/17/1999
POWDER FREE NITRILE EXAMINATION GLOVES
FLEXITECH SDN. BHD.
K990501
02/17/1999
POWDER FREE LATEX EXAMINATION GLOVES, W/ PROTEIN LABELING CLAIM
FLEXITECH SDN. BHD.
K994354
12/23/1999
POLYMER COATED, POWDER FREE, LATEX EXAMINATION GLOVES WITH PROTEIN CONTENT LABELING CLAIM (50 MICROGRAMS OR LESS)
FLEXITECH SDN. BHD.
K994416
12/29/1999
POLYMER COATED POWDER FREE NITRILE EXAMINATION GLOVES, BLUE
FLEXITECH SDN. BHD.
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