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510(k) FDA Premarket Notification K222709

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The following data is part of a premarket notification filed by with the FDA for .

Pre-market Notification Details

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Correspondent

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
08809495931002 K222709 000
08809495931316 K222709 000
08809495931323 K222709 000
08809495931330 K222709 000
08809495931347 K222709 000
08809495931354 K222709 000
08809495931361 K222709 000
08809495931378 K222709 000
08809495931385 K222709 000
08809495931095 K222709 000
08809495931101 K222709 000
08809495931156 K222709 000
08809495931163 K222709 000
08809495931170 K222709 000
08809495931187 K222709 000
08809495931194 K222709 000
08809495931200 K222709 000
08809495931293 K222709 000
08809495931309 K222709 000

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