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510(k) FDA Premarket Notification K231241

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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
00817493026055 K231241 000
00817493025850 K231241 000
00817493027748 K231241 000
00817493027731 K231241 000
00817493027724 K231241 000
00817493027717 K231241 000
00817493027700 K231241 000
00817493027694 K231241 000
00817493027687 K231241 000
00817493027670 K231241 000
00817493027328 K231241 000
00817493027311 K231241 000
00817493027304 K231241 000
00817493027298 K231241 000
00817493027281 K231241 000
00817493027274 K231241 000
00817493027267 K231241 000
00817493025867 K231241 000
00817493025874 K231241 000
00817493025881 K231241 000
00817493026048 K231241 000
00817493026031 K231241 000
00817493026024 K231241 000
00817493026017 K231241 000
00817493026000 K231241 000
00817493025997 K231241 000
00817493025980 K231241 000
00817493025973 K231241 000
00817493025966 K231241 000
00817493025959 K231241 000
00817493025942 K231241 000
00817493025935 K231241 000
00817493025928 K231241 000
00817493025911 K231241 000
00817493025904 K231241 000
00817493025898 K231241 000
00817493027250 K231241 000

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Line: 156
Function: _error_handler

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