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510(k) FDA Premarket Notification K230202

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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
M9461094261 K230202 000
M9461037251 K230202 000
M9461069270 K230202 000
M9461087570 K230202 000
M9461090000 K230202 000
M9461090030 K230202 000
M9461090040 K230202 000
M9461090050 K230202 000
M9461090600 K230202 000
M9461090790 K230202 000
M9461090910 K230202 000
M9461091010 K230202 000
M9461091260 K230202 000
M9461093430 K230202 000
M9461034491 K230202 000

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