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510(k) FDA Premarket Notification K242232

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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
07630542723841 K242232 000
07630542700606 K242232 000
07630542700613 K242232 000
07630542700620 K242232 000
07630542700637 K242232 000
07630542700644 K242232 000
07630542700651 K242232 000
07630542700668 K242232 000
07630542700675 K242232 000
07630542700682 K242232 000
07630542700699 K242232 000
07630542700590 K242232 000
07630542700583 K242232 000
07630542700484 K242232 000
07630542700491 K242232 000
07630542700507 K242232 000
07630542700514 K242232 000
07630542700521 K242232 000
07630542700538 K242232 000
07630542700545 K242232 000
07630542700552 K242232 000
07630542700569 K242232 000
07630542700576 K242232 000
07630542700705 K242232 000
07630542700712 K242232 000
07630542700729 K242232 000
07630542700859 K242232 000
07630542700866 K242232 000
07630542700873 K242232 000
07630542700880 K242232 000
07630542700897 K242232 000
07630542700903 K242232 000
07630542700910 K242232 000
07630542700927 K242232 000
07630542700934 K242232 000
07630542700460 K242232 000
07630542700842 K242232 000
07630542700835 K242232 000
07630542700736 K242232 000
07630542700743 K242232 000
07630542700750 K242232 000
07630542700767 K242232 000
07630542700774 K242232 000
07630542700781 K242232 000
07630542700798 K242232 000
07630542700804 K242232 000
07630542700811 K242232 000
07630542700828 K242232 000
07630542700477 K242232 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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