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510(k) FDA Premarket Notification K223883

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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
55060994741075 K223883 000
55060994741273 K223883 000
55060994741266 K223883 000
55060994741259 K223883 000
55060994741242 K223883 000
55060994741235 K223883 000
55060994741228 K223883 000
55060994741211 K223883 000
55060994741204 K223883 000
55060994741136 K223883 000
55060994741280 K223883 000
55060994741303 K223883 000
05060994740608 K223883 000
55060994740597 K223883 000
05060994741025 K223883 000
05060994741018 K223883 000
05060994741049 K223883 000
05060994741032 K223883 000
55060994741334 K223883 000
55060994741327 K223883 000
55060994741310 K223883 000
55060994741129 K223883 000

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