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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
06935650626468	K233140	000
06935650621333	K233140	000
06935650621357	K233140	000
06935650621371	K233140	000
06935650622613	K233140	000
06935650622620	K233140	000
06935650622637	K233140	000
06935650622651	K233140	000
06935650622668	K233140	000
06935650622682	K233140	000
06935650622699	K233140	000
06935650622729	K233140	000
06935650623344	K233140	000
06935650623351	K233140	000
06935650624327	K233140	000
06935650626048	K233140	000
06935650626451	K233140	000
06935650621319	K233140	000

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