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510(k) FDA Premarket Notification K223801

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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 IdentifiersubmissionNumberSupplement
03701037318515 K223801 000
03701037317891 K223801 000
03701037317907 K223801 000
03701037317914 K223801 000
03701037317921 K223801 000
03701037317938 K223801 000
03701037317945 K223801 000
03701037317952 K223801 000
03701037317969 K223801 000
03701037318423 K223801 000
03701037318430 K223801 000
03701037318447 K223801 000
03701037318454 K223801 000
03701037318461 K223801 000
03701037318478 K223801 000
03701037318485 K223801 000
03701037318492 K223801 000
03701037318508 K223801 000
03701037317884 K223801 000

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