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510(k) FDA Premarket Notification K241722

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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
05712821011213 K241722 000
05712821002471 K241722 000
05712821011220 K241722 000
05712821011237 K241722 000
05712821011244 K241722 000
05712821011251 K241722 000
05712821011275 K241722 000
05712821011282 K241722 000
05712821011527 K241722 000
05712821011572 K241722 000
05712821011992 K241722 000
05712821012036 K241722 000
05712821012890 K241722 000
05712821013415 K241722 000
05712821013422 K241722 000
05712821002389 K241722 000

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