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510(k) FDA Premarket Notification K231307

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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
05712821002532 K231307 000
05712821013767 K231307 000
05712821002006 K231307 000
05712821002013 K231307 000
05712821003072 K231307 000
05712821003096 K231307 000
05712821003119 K231307 000
05712821003133 K231307 000
05712821003157 K231307 000
05712821013750 K231307 000
05712821013354 K231307 000
05712821013347 K231307 000
05712821002556 K231307 000
05712821002570 K231307 000
05712821011602 K231307 000
05712821011619 K231307 000
05712821011626 K231307 000
05712821011633 K231307 000
05712821013323 K231307 000
05712821013330 K231307 000
05712821009562 K231307 000
05712821009586 K231307 000
05712821011985 K231307 000
05712821013361 K231307 000
05712821013378 K231307 000
05712821013385 K231307 000
05712821013392 K231307 000
05712821013408 K231307 000
05712821013514 K231307 000
05712821013521 K231307 000
05712821011978 K231307 000
05712821011961 K231307 000
05712821011954 K231307 000
05712821009609 K231307 000
05712821010490 K231307 000
05712821010506 K231307 000
05712821010513 K231307 000
05712821011817 K231307 000
05712821011824 K231307 000
05712821011916 K231307 000
05712821011947 K231307 000
05712821013538 K231307 000

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