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510(k) FDA Premarket Notification K220022

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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
00810149980930 K220022 000
00810149981388 K220022 000
00810149981340 K220022 000
00810149981326 K220022 000
00810149981449 K220022 000
00810149981357 K220022 000
00810149981418 K220022 000
00810149981296 K220022 000
00810149981272 K220022 000
00810149981425 K220022 000
00810149981463 K220022 000
00810149981333 K220022 000
00810149981319 K220022 000
00810149981371 K220022 000
00810149981364 K220022 000
00810149981401 K220022 000
00810149981289 K220022 000
00810149981432 K220022 000
00810149981456 K220022 000
00810149981395 K220022 000
00810149980497 K220022 000
00810149980084 K220022 000
00810149980015 K220022 000
00810149980992 K220022 000
00810149980978 K220022 000
00810149980954 K220022 000
00810149980633 K220022 000
00810149980619 K220022 000
00810149980596 K220022 000
00810149980572 K220022 000
00810149980558 K220022 000
00810149980534 K220022 000
00810149980510 K220022 000
00810149980107 K220022 000
00810149980060 K220022 000
00810149980046 K220022 000
00810149981302 K220022 000

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Function: _error_handler

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