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510(k) FDA Premarket Notification K223928

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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
06971008271218 K223928 000
06971008271225 K223928 000
06971008271232 K223928 000
06971008271249 K223928 000
06971008271089 K223928 000
06971008271096 K223928 000
06971008271102 K223928 000
06971008271119 K223928 000
06971008271126 K223928 000
06971008271133 K223928 000
06971008271140 K223928 000
06971008271157 K223928 000
06971008271164 K223928 000
06971008271171 K223928 000
06971008271188 K223928 000
06971008271195 K223928 000
06971008271201 K223928 000
06971008271263 K223928 000

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