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510(k) FDA Premarket Notification K233341

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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
20884521815329 K233341 000
20884521815237 K233341 000
20884521815244 K233341 000
30884521815258 K233341 000
30884521815265 K233341 000
20884521815275 K233341 000
20884521815282 K233341 000
30884521815296 K233341 000
20884521815305 K233341 000
20884521815312 K233341 000
20884521816272 K233341 000
30884521816286 K233341 000
30884521816293 K233341 000
20884521816302 K233341 000
30884521815227 K233341 000

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