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510(k) FDA Premarket Notification K232763

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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
08809559960931 K232763 000
08809295147108 K232763 000
08800142919190 K232763 000
08809295147481 K232763 000
08809295147474 K232763 000
08809295147467 K232763 000
08809295147450 K232763 000
08809295147443 K232763 000
08809295147436 K232763 000
08809295147429 K232763 000
08809295147412 K232763 000
08809295147405 K232763 000
08809295147399 K232763 000
08809295147382 K232763 000
08800142919220 K232763 000
08800142919213 K232763 000
08809295147115 K232763 000
08809295147122 K232763 000
08809295147375 K232763 000
08809295147368 K232763 000
08809295147351 K232763 000
08809295147344 K232763 000
08809295147337 K232763 000
08809295147320 K232763 000
08809295147313 K232763 000
08809295147306 K232763 000
08809295147290 K232763 000
08809295147283 K232763 000
08809295147177 K232763 000
08809295147160 K232763 000
08809295147153 K232763 000
08809295147146 K232763 000
08809295147139 K232763 000
08800142919206 K232763 000

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Filename: fda.report/pmn_item.php

Line Number: 156

Backtrace:

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Line: 156
Function: _error_handler


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