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510(k) FDA Premarket Notification K223332

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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
09120073932310 K223332 000
09120073932433 K223332 000
09120073932365 K223332 000
09120073932341 K223332 000
09120073932334 K223332 000
09120073932327 K223332 000
09120073932303 K223332 000
09120073932297 K223332 000
09120073932280 K223332 000
09120073932440 K223332 000
09120073932457 K223332 000
09120073932464 K223332 000
09120073932983 K223332 000
09120073932976 K223332 000
09120073932969 K223332 000
09120073932952 K223332 000
09120073932945 K223332 000
09120073932938 K223332 000
09120073932716 K223332 000
09120073932471 K223332 000
09120073932273 K223332 000

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