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510(k) FDA Premarket Notification K241224

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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
10197344157549 K241224 000
10197344157419 K241224 000
10197344157402 K241224 000
10197344157396 K241224 000
10197344157389 K241224 000
10197344157372 K241224 000
10197344157365 K241224 000
10197344157358 K241224 000
10197344157341 K241224 000
10197344157334 K241224 000
10197344157327 K241224 000
10197344157426 K241224 000
10197344157433 K241224 000
10197344157532 K241224 000
10197344157525 K241224 000
10197344157518 K241224 000
10197344157501 K241224 000
10197344157495 K241224 000
10197344157488 K241224 000
10197344157471 K241224 000
10197344157464 K241224 000
10197344157457 K241224 000
10197344157440 K241224 000
10197344157310 K241224 000

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