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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
07332747111972	K153534	000
07332747179576	K153534	000
07332747179583	K153534	000
07332747179590	K153534	000
07332747179613	K153534	000
07332747179620	K153534	000
07332747179958	K153534	000
07332747179965	K153534	000
07332747179989	K153534	000
07332747180015	K153534	000
07332747111927	K153534	000
07332747111934	K153534	000
07332747111941	K153534	000
07332747111958	K153534	000
07332747111965	K153534	000
07332747179569	K153534	000

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