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510(k) FDA Premarket Notification K240201

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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
08806344398429 K240201 000
08806344398566 K240201 000
08806344398573 K240201 000
08806344398580 K240201 000
08806344398597 K240201 000
08806344398603 K240201 000
08806344398610 K240201 000
08806344398627 K240201 000
08806344398634 K240201 000
08806344398641 K240201 000
08806344398658 K240201 000
08806344398559 K240201 000
08806344398542 K240201 000
08806344398535 K240201 000
08806344398436 K240201 000
08806344398443 K240201 000
08806344398450 K240201 000
08806344398467 K240201 000
08806344398474 K240201 000
08806344398481 K240201 000
08806344398498 K240201 000
08806344398504 K240201 000
08806344398511 K240201 000
08806344398528 K240201 000
08806344398368 K240201 000
08806344398375 K240201 000
08806344398382 K240201 000
08806344398252 K240201 000
08806344398269 K240201 000
08806344398276 K240201 000
08806344398283 K240201 000
08806344398290 K240201 000
08806344398306 K240201 000
08806344398313 K240201 000
08806344398320 K240201 000
08806344398337 K240201 000
08806344398344 K240201 000
08806344398245 K240201 000
08806344398238 K240201 000
08806344398221 K240201 000
08806344398399 K240201 000
08806344398405 K240201 000
08806344398412 K240201 000
08806344398153 K240201 000
08806344398160 K240201 000
08806344398177 K240201 000
08806344398184 K240201 000
08806344398191 K240201 000
08806344398207 K240201 000
08806344398214 K240201 000
08806344398351 K240201 000

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Filename: fda.report/pmn_item.php

Line Number: 156

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Line: 156
Function: _error_handler


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