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510(k) FDA Premarket Notification K153534

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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
07332747111972 K153534 000
07332747179576 K153534 000
07332747179583 K153534 000
07332747179590 K153534 000
07332747179613 K153534 000
07332747179620 K153534 000
07332747179958 K153534 000
07332747179965 K153534 000
07332747179989 K153534 000
07332747180015 K153534 000
07332747111927 K153534 000
07332747111934 K153534 000
07332747111941 K153534 000
07332747111958 K153534 000
07332747111965 K153534 000
07332747179569 K153534 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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