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510(k) FDA Premarket Notification K231232

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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
B648C1054404P0 K231232 000
B648C10542310SD0 K231232 000
B648C10542308ST0 K231232 000
B648C10542308SD0 K231232 000
B648C10542306ST0 K231232 000
B648C10542306SD0 K231232 000
B648C10542304ST0 K231232 000
B648C1054112SS0 K231232 000
B648C1054112N0 K231232 000
B648C1054110SS0 K231232 000
B648C1054110N0 K231232 000
B648C1054108SS0 K231232 000
B648C1054108N0 K231232 000
B648C1054106SS0 K231232 000
B648C1054106N0 K231232 000
B648C10542310ST0 K231232 000
B648C10542312SD0 K231232 000
B648C10542304SD0 K231232 000
B648C1054104N0 K231232 000
B648C1054412P0 K231232 000
B648C1054410P0 K231232 000
B648C1054408P0 K231232 000
B648C1054406P0 K231232 000
B648C10543SS0 K231232 000
B648C10543N0 K231232 000
B648C10542712ST0 K231232 000
B648C10542710ST0 K231232 000
B648C10542708ST0 K231232 000
B648C10542706ST0 K231232 000
B648C10542704ST0 K231232 000
B648C10542312ST0 K231232 000
B648C1054104SS0 K231232 000

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Line: 156
Function: _error_handler

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