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510(k) FDA Premarket Notification K233524

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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
10610075092762 K233524 000
10610075092960 K233524 000
10610075094483 K233524 000
10610075094476 K233524 000
10610075094469 K233524 000
10610075094445 K233524 000
10610075094438 K233524 000
10610075094421 K233524 000
10610075094407 K233524 000
10610075094391 K233524 000
10610075092977 K233524 000
10610075092984 K233524 000
10610075092991 K233524 000
10610075092755 K233524 000
10610075092748 K233524 000
10610075092731 K233524 000
10610075092724 K233524 000
10610075092717 K233524 000
10610075093080 K233524 000
10610075093073 K233524 000
10610075093066 K233524 000
10610075093059 K233524 000
10610075094384 K233524 000

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