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What the FDA does require, however, is for manufacturers of all examination (medical grade) gloves to have 510(k) device listings on file with the agency. This means that the manufacturer has been tested and approved to manufacture gloves for medical use (typically involves ISO certification, as well).
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What the FDA does require, however, is for manufacturers of all examination (medical grade) gloves to have 510(k) device listings on file with the agency. This means that the manufacturer has been tested and approved to manufacture gloves for medical use (typically involves ISO certification, as well).
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