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510(k) FDA Premarket Notification K242703

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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
08809918255272 K242703 000
08809918209763 K242703 000
08809918209770 K242703 000
08809918209787 K242703 000
08809918209794 K242703 000
08809918209800 K242703 000
08809918209817 K242703 000
08809918209824 K242703 000
08809918255203 K242703 000
08809918255210 K242703 000
08809918255227 K242703 000
08809918255234 K242703 000
08809918255241 K242703 000
08809918255258 K242703 000
08809918255265 K242703 000
08809918209756 K242703 000

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