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510(k) FDA Premarket Notification K231961

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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
06972820967525 K231961 000
06942108005546 K231961 000
06942108005553 K231961 000
06942108005560 K231961 000
06972820961509 K231961 000
06972820961516 K231961 000
06972820961523 K231961 000
06972820961530 K231961 000
06972820961691 K231961 000
06972820963442 K231961 000
06972820963459 K231961 000
06972820963497 K231961 000
06972820963893 K231961 000
06972820967457 K231961 000
06972820967488 K231961 000
06972820967518 K231961 000
06972820963602 K231961 000

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