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510(k) FDA Premarket Notification K242260

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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
00810056992996 K242260 000
00810056992491 K242260 000
00810056992460 K242260 000
00810056992453 K242260 000
00810056992422 K242260 000
00810056992415 K242260 000
00810056992385 K242260 000
00810056992378 K242260 000
00810056992347 K242260 000
00810056992330 K242260 000
00810056992507 K242260 000
00810056992538 K242260 000
00810056992545 K242260 000
00810056992989 K242260 000
00810056992965 K242260 000
00810056992873 K242260 000
00810056992811 K242260 000
00810056992750 K242260 000
00810056992620 K242260 000
00810056992613 K242260 000
00810056992583 K242260 000
00810056992576 K242260 000
00810056991869 K242260 000

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