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510(k) FDA Premarket Notification K231055

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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
D804592151030 K231055 000
D804592151000 K231055 000
D804592151010 K231055 000
D804592151020 K231055 000
D804592151070 K231055 000
D804592151080 K231055 000
D804592151090 K231055 000
D804592151100 K231055 000
D804592151110 K231055 000
D804592151120 K231055 000
D804592151170 K231055 000
D804592151180 K231055 000
D804592151190 K231055 000
D804593151080 K231055 000
D804592151130 K231055 000
D804592159850 K231055 000
D804592159900 K231055 000
03760262652993 K231055 000

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