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510(k) FDA Premarket Notification K231389

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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
D870S979520 K231389 000
D87098541 K231389 000
D87098521 K231389 000
D87098501 K231389 000
D87098481 K231389 000
D87098461 K231389 000
D87098441 K231389 000
D87098421 K231389 000
D87098401 K231389 000
D87098561 K231389 000
D87098581 K231389 000
D87098361 K231389 000
D870981225 K231389 000
D870981023 K231389 000
D87098082 K231389 000
D870980628 K231389 000
D870980426 K231389 000
D87097972 K231389 000
D87098601 K231389 000
D870980011 K231389 000

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