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510(k) FDA Premarket Notification K250317

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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
08809262950007 K250317 000
08809262950168 K250317 000
08809262950175 K250317 000
08809262950182 K250317 000
08809262950199 K250317 000
08809262950212 K250317 000
08809262950229 K250317 000
08809262950236 K250317 000
08809262950243 K250317 000
08809262950250 K250317 000
08809262950267 K250317 000
08809262950274 K250317 000
08809262950281 K250317 000
08809262950298 K250317 000
08809262950151 K250317 000
08809262950144 K250317 000
08809262950014 K250317 000
08809262950021 K250317 000
08809262950038 K250317 000
08809262950045 K250317 000
08809262950052 K250317 000
08809262950069 K250317 000
08809262950076 K250317 000
08809262950083 K250317 000
08809262950090 K250317 000
08809262950106 K250317 000
08809262950113 K250317 000
08809262950120 K250317 000
08809262950137 K250317 000
08809262950304 K250317 000
08809262950311 K250317 000
08809262950489 K250317 000
08809262950496 K250317 000
08809262950502 K250317 000
08809262950519 K250317 000
08809262950526 K250317 000
08809262950533 K250317 000
08809262950540 K250317 000
08809262950557 K250317 000
08809262950564 K250317 000
08809262950571 K250317 000
08809262950588 K250317 000
08809262950595 K250317 000
08809262950601 K250317 000
08809262950472 K250317 000
08809262950465 K250317 000
08809262950328 K250317 000
08809262950335 K250317 000
08809262950342 K250317 000
08809262950359 K250317 000
08809262950366 K250317 000
08809262950373 K250317 000
08809262950380 K250317 000
08809262950397 K250317 000
08809262950403 K250317 000
08809262950427 K250317 000
08809262950434 K250317 000
08809262950441 K250317 000
08809262950458 K250317 000
08809262950618 K250317 000

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Severity: Notice

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Filename: fda.report/pmn_item.php

Line Number: 156

Backtrace:

File: /var/www/fda.report/pmn_item.php
Line: 156
Function: _error_handler


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