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510(k) FDA Premarket Notification K220157

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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
16932503531242 K220157 000
16932503531112 K220157 000
16932503531105 K220157 000
16932503531099 K220157 000
16932503531082 K220157 000
16932503531075 K220157 000
16932503531068 K220157 000
16932503531051 K220157 000
16932503531044 K220157 000
16932503531037 K220157 000
16932503531020 K220157 000
16932503531129 K220157 000
16932503531136 K220157 000
16932503531235 K220157 000
16932503531228 K220157 000
16932503531211 K220157 000
16932503531204 K220157 000
16932503531198 K220157 000
16932503531181 K220157 000
16932503531174 K220157 000
16932503531167 K220157 000
16932503531150 K220157 000
16932503531143 K220157 000
16932503531013 K220157 000

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