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510(k) FDA Premarket Notification K230565

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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
00193982565312 K230565 000
00193982506445 K230565 000
00193982506292 K230565 000
00193982506285 K230565 000
00193982506278 K230565 000
00193982506261 K230565 000
00193982506254 K230565 000
00193982506247 K230565 000
00193982506230 K230565 000
00193982506223 K230565 000
00193982506452 K230565 000
00193982506469 K230565 000
00193982565305 K230565 000
00193982565299 K230565 000
00193982518837 K230565 000
00193982506544 K230565 000
00193982506537 K230565 000
00193982506520 K230565 000
00193982506513 K230565 000
00193982506490 K230565 000
00193982506476 K230565 000
00193982506216 K230565 000

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