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510(k) FDA Premarket Notification K230505

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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
06430035875108 K230505 000
06430035875092 K230505 000
06430035875139 K230505 000
06430035875177 K230505 000

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