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510(k) FDA Premarket Notification K250598

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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
09421908222263 K250598 000
09421907331881 K250598 000
09421907331928 K250598 000
09421907331935 K250598 000
09421907331942 K250598 000
09421907331959 K250598 000
09421907331966 K250598 000
09421907331973 K250598 000
09421907331997 K250598 000
09421908222065 K250598 000
09421908222072 K250598 000
09421908222089 K250598 000
09421908222096 K250598 000
09421908222102 K250598 000
09421908222119 K250598 000
09421908222126 K250598 000
09421908222140 K250598 000
09421908222157 K250598 000
09421907331874 K250598 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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