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510(k) FDA Premarket Notification K240393

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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
10885862607812 K240393 000
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10885862608222 K240393 000
10885862608215 K240393 000
10885862608079 K240393 000
10885862608062 K240393 000
10885862607928 K240393 000
10885862607911 K240393 000
10885862607904 K240393 000
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10885862608000 K240393 000
10885862607997 K240393 000
10885862607980 K240393 000
10885862607973 K240393 000
10885862607966 K240393 000
10885862607829 K240393 000

A PHP Error was encountered

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Line: 156
Function: _error_handler


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