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510(k) FDA Premarket Notification K192481

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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
08800061399974 K192481 000
08800061643596 K192481 000
08800061643602 K192481 000
08800061643664 K192481 000
08800061643671 K192481 000
08800061643688 K192481 000
08800061643909 K192481 000
08800061643916 K192481 000
08800061643923 K192481 000
08800061643985 K192481 000
08800061643992 K192481 000
08800061644005 K192481 000
08800061399929 K192481 000
08800061399936 K192481 000
08800061399943 K192481 000
08800061399950 K192481 000
08800061399967 K192481 000
08800061643589 K192481 000

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