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510(k) FDA Premarket Notification K233811

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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
00850054882219 K233811 000
00850054882097 K233811 000
00850054882080 K233811 000
00850054882073 K233811 000
00850054882066 K233811 000
00850054882059 K233811 000
00850054882042 K233811 000
00810182930084 K233811 000
00810182930077 K233811 000
00850054882103 K233811 000
00850054882110 K233811 000
00850054882127 K233811 000
00850054882202 K233811 000
00850054882196 K233811 000
00850054882189 K233811 000
00850054882172 K233811 000
00850054882165 K233811 000
00850054882158 K233811 000
00850054882141 K233811 000
00850054882134 K233811 000
00810182930060 K233811 000

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Filename: fda.report/pmn_item.php

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