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510(k) FDA Premarket Notification K243732

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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
08436568735511 K243732 000
08436568734354 K243732 000
08436568734347 K243732 000
08436568734330 K243732 000
08436568734323 K243732 000
08436568734316 K243732 000
08436568734309 K243732 000
08436568734293 K243732 000
08436568734286 K243732 000
08436568733975 K243732 000
08436568733968 K243732 000
08436568733951 K243732 000
08436568733944 K243732 000
08436568733876 K243732 000
08436568733869 K243732 000
08436568733852 K243732 000
08436568733845 K243732 000
08436568734651 K243732 000
08436568734668 K243732 000
08436568734675 K243732 000
08436568735504 K243732 000
08436568735498 K243732 000
08436568735481 K243732 000
08436568735474 K243732 000
08436568735467 K243732 000
08436568735450 K243732 000
08436568735443 K243732 000
08436568734767 K243732 000
08436568734750 K243732 000
08436568734743 K243732 000
08436568734736 K243732 000
08436568734729 K243732 000
08436568734712 K243732 000
08436568734705 K243732 000
08436568734699 K243732 000
08436568734682 K243732 000
08435673512277 K243732 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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