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510(k) FDA Premarket Notification K230398

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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
00810007632698 K230398 000
00810007632544 K230398 000
00810007632537 K230398 000
00810007632520 K230398 000
00810007632513 K230398 000
00810007632506 K230398 000
00810007632490 K230398 000
00810007632483 K230398 000
00810007632476 K230398 000
00810007632469 K230398 000
00810007632582 K230398 000
00810007632711 K230398 000
00810007632551 K230398 000
00810007632568 K230398 000
00810007632681 K230398 000
00810007632674 K230398 000
00810007632667 K230398 000
00810007632650 K230398 000
00810007632643 K230398 000
00810007632636 K230398 000
00810007632629 K230398 000
00810007632612 K230398 000
00810007632605 K230398 000
00810007632599 K230398 000
00810007632575 K230398 000
00810007632704 K230398 000

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