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510(k) FDA Premarket Notification K233482

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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
10885862631657 K233482 000
10885862657053 K233482 000
10885862657237 K233482 000
10885862625618 K233482 000
10885862625625 K233482 000
10885862625632 K233482 000
10885862625649 K233482 000
10885862625656 K233482 000
10885862625663 K233482 000
10885862630384 K233482 000
10885862631565 K233482 000
10885862631589 K233482 000
10885862631596 K233482 000
10885862631602 K233482 000
10885862631619 K233482 000
10885862631626 K233482 000
10885862631633 K233482 000
10885862631640 K233482 000
10885862657046 K233482 000

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