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510(k) FDA Premarket Notification K241063

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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
08800053071307 K241063 000
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08800053070553 K241063 000
08800053071963 K241063 000
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08800053071734 K241063 000
08800053071727 K241063 000
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08800053071703 K241063 000
08800053071697 K241063 000
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08800053071451 K241063 000
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Line: 156
Function: _error_handler


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