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510(k) FDA Premarket Notification K233735

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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
00193982535902 K233735 000
00193982535742 K233735 000
00193982535735 K233735 000
00193982535728 K233735 000
00193982535711 K233735 000
00193982535704 K233735 000
00193982535698 K233735 000
00193982535681 K233735 000
00193982535667 K233735 000
00193982535643 K233735 000
00193982535636 K233735 000
00193982615611 K233735 000
00193982535759 K233735 000
00193982535766 K233735 000
00193982535773 K233735 000
00193982535896 K233735 000
00193982535889 K233735 000
00193982535872 K233735 000
00193982535865 K233735 000
00193982535841 K233735 000
00193982535834 K233735 000
00193982535827 K233735 000
00193982535810 K233735 000
00193982535803 K233735 000
00193982535797 K233735 000
00193982535780 K233735 000
00193982615604 K233735 000

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