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510(k) FDA Premarket Notification K233389

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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
00810125999222 K233389 000
00810125999369 K233389 000
00810125999376 K233389 000
00810125999383 K233389 000
00810125999390 K233389 000
00810125999406 K233389 000
00810125999413 K233389 000
00810125999420 K233389 000
00810125999437 K233389 000
00810125999444 K233389 000
00810125999451 K233389 000
00810125999468 K233389 000
00810125999352 K233389 000
00810125999345 K233389 000
00810125999239 K233389 000
00810125999246 K233389 000
00810125999253 K233389 000
00810125999260 K233389 000
00810125999277 K233389 000
00810125999284 K233389 000
00810125999291 K233389 000
00810125999307 K233389 000
00810125999314 K233389 000
00810125999321 K233389 000
00810125999338 K233389 000
00810125999475 K233389 000
00810125999482 K233389 000
00810125999635 K233389 000
00810125999642 K233389 000
00810125999659 K233389 000
00810125999666 K233389 000
00810125999673 K233389 000
00810125999680 K233389 000
00810125999697 K233389 000
00810125999536 K233389 000
00810125999154 K233389 000
00810125999161 K233389 000
00810125999178 K233389 000
00810125999628 K233389 000
00810125999611 K233389 000
00810125999499 K233389 000
00810125999505 K233389 000
00810125999512 K233389 000
00810125999529 K233389 000
00810125999543 K233389 000
00810125999550 K233389 000
00810125999567 K233389 000
00810125999574 K233389 000
00810125999581 K233389 000
00810125999598 K233389 000
00810125999604 K233389 000
00810125999185 K233389 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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