510(k) FDA Premarket Notification K200272

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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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Correspondent

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
07798164679295	K200272	000
07798164678847	K200272	000
07798164677871	K200272	000
07798375770224	K200272	000
07798375772198	K200272	000
07798375772754	K200272	000
07798375772532	K200272	000

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