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510(k) FDA Premarket Notification K220309

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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
06975740360117 K220309 000
06975740369233 K220309 000
06975740369257 K220309 000
06975740369271 K220309 000
06975740369172 K220309 000
06975740369196 K220309 000
06975740369059 K220309 000
06975740369035 K220309 000
06975740369011 K220309 000
06975740369073 K220309 000
06975740369158 K220309 000
06975740369141 K220309 000
06975740369110 K220309 000
06975740369165 K220309 000
06975740369134 K220309 000
06975740369127 K220309 000
06975740369103 K220309 000
06975740369097 K220309 000
06975740369219 K220309 000

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