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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
08800053098823	K240511	000
08800053098700	K240511	000
08800053098694	K240511	000
08800053098687	K240511	000
08800053098670	K240511	000
08800053098663	K240511	000
08800053098656	K240511	000
08800053098649	K240511	000
08800053098632	K240511	000
08800053098717	K240511	000
08800053098724	K240511	000
08800053098816	K240511	000
08800053098809	K240511	000
08800053098793	K240511	000
08800053098786	K240511	000
08800053098779	K240511	000
08800053098762	K240511	000
08800053098748	K240511	000
08800053098731	K240511	000
08800053098625	K240511	000

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