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510(k) FDA Premarket Notification K211785

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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
00841732167315 K211785 000
00841732131576 K211785 000
00841732131569 K211785 000
00841732131552 K211785 000
00841732131545 K211785 000
00841732131538 K211785 000
00841732131521 K211785 000
00841732131514 K211785 000
00841732131507 K211785 000
00841732131491 K211785 000
00841732131484 K211785 000
00841732129634 K211785 000
00841732129627 K211785 000
00841732129610 K211785 000
00841732129597 K211785 000
00841732129580 K211785 000
00841732131583 K211785 000
00841732131590 K211785 000
00841732144347 K211785 000
00841732131606 K211785 000
00841732129603 K211785 000
00841732145726 K211785 000
00841732145719 K211785 000
00841732145702 K211785 000
00841732144330 K211785 000
00841732144323 K211785 000
00841732144316 K211785 000
00841732134355 K211785 000
00841732134348 K211785 000
00841732131651 K211785 000
00841732131613 K211785 000
00841732129566 K211785 000
00841732129559 K211785 000
00841732129542 K211785 000
00841732129573 K211785 000

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