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510(k) FDA Premarket Notification K240392

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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
03607506353950 K240392 000
03607506336007 K240392 000
03607506335994 K240392 000
03607506335925 K240392 000
03607506313442 K240392 000
03607506313435 K240392 000
03607506313428 K240392 000
03607506313411 K240392 000
03607506313398 K240392 000
03607506313374 K240392 000
03607506310526 K240392 000
03607506310519 K240392 000
03607506336014 K240392 000
03607506336021 K240392 000
03607506348284 K240392 000
03607506343777 K240392 000
03607506343760 K240392 000
03607506343753 K240392 000
03607506343746 K240392 000
03607506343654 K240392 000
03607506343647 K240392 000
03607506336144 K240392 000
03607506336137 K240392 000
03607506336120 K240392 000
03607506336038 K240392 000
03607506310502 K240392 000

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