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510(k) FDA Premarket Notification K212703

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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
07290117771839 K212703 000
07290117771396 K212703 000
07290117771402 K212703 000
07290117771419 K212703 000
07290117771426 K212703 000
07290117771433 K212703 000
07290117771440 K212703 000
07290117771457 K212703 000
07290117771464 K212703 000
07290117771471 K212703 000
07290117771488 K212703 000
07290117771495 K212703 000
07290117771525 K212703 000
07290117771532 K212703 000
07290117771549 K212703 000
07290117772355 K212703 000
07290117771822 K212703 000
07290117771372 K212703 000

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