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510(k) FDA Premarket Notification K233694

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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
10889981310448 K233694 000
10889981326401 K233694 000
10889981326395 K233694 000
10889981326388 K233694 000
10889981326371 K233694 000
10889981326364 K233694 000
10889981326357 K233694 000
10889981326340 K233694 000
10889981326333 K233694 000
10889981326326 K233694 000
10889981326319 K233694 000
10889981326302 K233694 000
10889981326296 K233694 000
10889981326289 K233694 000
10889981326272 K233694 000
10889981326418 K233694 000
10889981326425 K233694 000
10889981326432 K233694 000
10889981310431 K233694 000
10889981310424 K233694 000
10889981310417 K233694 000
10889981310400 K233694 000
10889981310394 K233694 000
10889981310387 K233694 000
10889981310370 K233694 000
10889981310363 K233694 000
10889981310356 K233694 000
10889981325107 K233694 000
10889981325091 K233694 000
10889981326463 K233694 000
10889981326456 K233694 000
10889981326449 K233694 000
10889981326265 K233694 000

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Filename: fda.report/pmn_item.php

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