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510(k) FDA Premarket Notification K230971

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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
07630894802935 K230971 000
07630894801402 K230971 000
07630894801396 K230971 000
07630894801389 K230971 000
07630894801372 K230971 000
07630894801365 K230971 000
07630894801358 K230971 000
07630894801341 K230971 000
07630894801327 K230971 000
07630894801310 K230971 000
07630894801297 K230971 000
07630894801280 K230971 000
07630894801273 K230971 000
07630894800849 K230971 000
07630894800832 K230971 000
07630894800825 K230971 000
07630894801419 K230971 000
07630894801426 K230971 000
07630894801433 K230971 000
07630037856269 K230971 000
07630894801303 K230971 000
07630894802492 K230971 000
07630894802485 K230971 000
07630894802478 K230971 000
07630894802461 K230971 000
07630894802454 K230971 000
07630894802447 K230971 000
07630894802430 K230971 000
07630894802423 K230971 000
07630894802416 K230971 000
07630894802409 K230971 000
07630894802393 K230971 000
07630894801471 K230971 000
07630894801440 K230971 000
07630894800818 K230971 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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