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510(k) FDA Premarket Notification K231347

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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
D745701123BRX00410 K231347 000
D745701123BRX00260 K231347 000
D745701123BRX00270 K231347 000
D745701123BRX00280 K231347 000
D745701123BRX00290 K231347 000
D745701123BRX00300 K231347 000
D745701123BRX00340 K231347 000
D745701123BRX00350 K231347 000
D745701123BRX00360 K231347 000
D745701123BRX00370 K231347 000
D745701123BRX00380 K231347 000
D745701123BRX00390 K231347 000
D745701123BRX00400 K231347 000
D745701123BRX00250 K231347 000

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