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510(k) FDA Premarket Notification K220478

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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
00195377061744 K220478 000
00195377056122 K220478 000
00195377056115 K220478 000
00195377056108 K220478 000
00195377055590 K220478 000
00195377055583 K220478 000
00195377055576 K220478 000
00195377055569 K220478 000
00195377043535 K220478 000
00195377043511 K220478 000
00195377042163 K220478 000
00195377056139 K220478 000
00195377056146 K220478 000
00195377061737 K220478 000
00195377056238 K220478 000
00195377056221 K220478 000
00195377056214 K220478 000
00195377056207 K220478 000
00195377056191 K220478 000
00195377056184 K220478 000
00195377056177 K220478 000
00195377056160 K220478 000
00195377056153 K220478 000
00195377042132 K220478 000

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Filename: fda.report/pmn_item.php

Line Number: 156

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