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510(k) FDA Premarket Notification K242432

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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
E322051200652020 K242432 000
E322031202440 K242432 000
E322048000101010 K242432 000
E322048000091010 K242432 000
E322048000081010 K242432 000
E322048000071010 K242432 000
E322048000061010 K242432 000
E322048000051010 K242432 000
E322048000041010 K242432 000
E322048000031010 K242432 000
E322048000021010 K242432 000
E322031202450 K242432 000
E322040001320 K242432 000
E322029001700010 K242432 000
E322048000100 K242432 000
E322048000090 K242432 000
E322048000080 K242432 000
E322048000070 K242432 000
E322048000060 K242432 000
E322048000050 K242432 000
E322048000040 K242432 000
E322048000030 K242432 000
E322048000020 K242432 000
E322048000010 K242432 000
E322048000011010 K242432 000

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