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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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NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
00810024671106	K242106	000
00810024670512	K242106	000
00810024670529	K242106	000
00810024670567	K242106	000
00810024670574	K242106	000
00810024670581	K242106	000
00810024670680	K242106	000
00810024670697	K242106	000
00810024670703	K242106	000
00810024670710	K242106	000
00810024670727	K242106	000
00810024670734	K242106	000
00810024670741	K242106	000
00810024670758	K242106	000
00810024670765	K242106	000
00810024670840	K242106	000
00810024671090	K242106	000
00810024670505	K242106	000

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