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510(k) FDA Premarket Notification K242445

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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
07613327625127 K242445 000
07613327624854 K242445 000
07613327624823 K242445 000
07613327624793 K242445 000
07613327624779 K242445 000
07613327625035 K242445 000
07613327624991 K242445 000
07613327624984 K242445 000
07613327624977 K242445 000
07613327624892 K242445 000
07613327624922 K242445 000
07613327625110 K242445 000
07613327625103 K242445 000
07613327625097 K242445 000
07613327625073 K242445 000
07613327625004 K242445 000
07613327624960 K242445 000
07613327624953 K242445 000
07613327624946 K242445 000
07613327624830 K242445 000

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Filename: fda.report/pmn_item.php

Line Number: 156

Backtrace:

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Line: 156
Function: _error_handler

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