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510(k) FDA Premarket Notification K230317

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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
05712821000309 K230317 000
05712821000460 K230317 000
05712821000552 K230317 000
05712821000569 K230317 000
05712821001290 K230317 000
05712821001306 K230317 000
05712821001313 K230317 000
05712821001320 K230317 000
05712821001337 K230317 000
05712821002273 K230317 000
05712821000453 K230317 000
05712821000446 K230317 000
05712821013644 K230317 000
05712821000316 K230317 000
05712821000323 K230317 000
05712821000330 K230317 000
05712821007797 K230317 000
05712821007803 K230317 000
05712821007810 K230317 000
05712821007827 K230317 000
05712821013743 K230317 000
05712821013637 K230317 000
05712821002341 K230317 000
05712821007964 K230317 000
05712821007971 K230317 000
05712821010421 K230317 000
05712821010438 K230317 000
05712821010445 K230317 000
05712821010452 K230317 000
05712821010469 K230317 000
05712821010476 K230317 000
05712821010483 K230317 000
05712821010520 K230317 000
05712821010537 K230317 000
05712821010414 K230317 000
05712821010407 K230317 000
05712821010391 K230317 000
05712821007988 K230317 000
05712821007995 K230317 000
05712821008008 K230317 000
05712821008220 K230317 000
05712821008237 K230317 000
05712821008244 K230317 000
05712821008251 K230317 000
05712821008268 K230317 000
05712821010384 K230317 000
05712821010544 K230317 000

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