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510(k) FDA Premarket Notification K240698

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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
30850065976595 K240698 000
30850065976069 K240698 000
00850065976075 K240698 000
30850065976083 K240698 000
00850065976099 K240698 000
00850065976235 K240698 000
30850065976243 K240698 000
30850065976250 K240698 000
30850065976274 K240698 000
30850065976458 K240698 000
30850065976465 K240698 000
30850065976472 K240698 000
30850065976489 K240698 000
30850065976496 K240698 000
30850065976502 K240698 000
30850065976519 K240698 000
30850065976557 K240698 000
00850054867698 K240698 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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