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510(k) FDA Premarket Notification K230663

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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
08800020104304 K230663 000
08800020103918 K230663 000
08800020103925 K230663 000
08800020103932 K230663 000
08800020103949 K230663 000
08800020103956 K230663 000
08800020103963 K230663 000
08800020103970 K230663 000
08800020103987 K230663 000
08800020104229 K230663 000
08800020104236 K230663 000
08800020104243 K230663 000
08800020104250 K230663 000
08800020104267 K230663 000
08800020104274 K230663 000
08800020104281 K230663 000
08800020104298 K230663 000
08800020103536 K230663 000

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