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510(k) FDA Premarket Notification K242744

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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
05056139252181 K242744 000
05056139252082 K242744 000
05056139252075 K242744 000
05056139252068 K242744 000
05056139252051 K242744 000
05056139248849 K242744 000
05056139248832 K242744 000
05056139252211 K242744 000
05056139252204 K242744 000
05056139252099 K242744 000
05056139252105 K242744 000
05056139252433 K242744 000
05056139252174 K242744 000
05056139252167 K242744 000
05056139252150 K242744 000
05056139252143 K242744 000
05056139252136 K242744 000
05056139252129 K242744 000
05056139252112 K242744 000
05056139252198 K242744 000

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Filename: fda.report/pmn_item.php

Line Number: 156

Backtrace:

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