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510(k) FDA Premarket Notification K220703

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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
09420012466747 K220703 000
09420012461049 K220703 000
09420012461230 K220703 000
09420012461292 K220703 000
09420012466693 K220703 000
09420012450012 K220703 000
09420012456625 K220703 000
09420012461223 K220703 000
09420012461247 K220703 000
09420012461254 K220703 000
09420012461261 K220703 000
09420012461278 K220703 000
09420012461315 K220703 000
09420012461322 K220703 000
09420012465726 K220703 000
09420012465719 K220703 000
09420012474315 K220703 000

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