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PHILIPS JUN 122014 510(k) Summary of Safety and Effectiveness This 510(k) summary of safety and effectiveness information is prepared in accordance with 21 CFR 807.92. Date Prepared: March 21, 2014,

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1. Individuals or organizations interested in obtaining information about Philips products regulated by the FDA.
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What is philips - accessdatafdagov?

Philips - Accessdatafdagov is a database used by the FDA to collect information on Philips medical devices.

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Manufacturers of Philips medical devices are required to file information on Philips - Accessdatafdagov.

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Information such as product name, manufacturer details, device classification, and reported adverse events must be reported on Philips - Accessdatafdagov.