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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
08435750428255	K242340	000
08435750427623	K242340	000
08435750427630	K242340	000
08435750427647	K242340	000
08435750427654	K242340	000
08435750427661	K242340	000
08435750427678	K242340	000
08435750427685	K242340	000
08435750427692	K242340	000
08435750427708	K242340	000
08435750427715	K242340	000
08435750427722	K242340	000
08435750426718	K242340	000
08435750426725	K242340	000
08435750428033	K242340	000
08435750428224	K242340	000
08435750427616	K242340	000

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