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510(k) FDA Premarket Notification K213217

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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
06934415012072 K213217 000
06934415012133 K213217 000
06934415012126 K213217 000
06934415012119 K213217 000
06934415012102 K213217 000
06934415012096 K213217 000
06934415012089 K213217 000
06934415012065 K213217 000
06934415012058 K213217 000
06934415012041 K213217 000
06934415012027 K213217 000
06934415012010 K213217 000
06934415012003 K213217 000
06934415011198 K213217 000
06934415012140 K213217 000
06934415012171 K213217 000
06934415012034 K213217 000
06934415011266 K213217 000
06934415011259 K213217 000
06934415011242 K213217 000
06934415011143 K213217 000
06934415011129 K213217 000
06934415011105 K213217 000
06934415012164 K213217 000
06934415012157 K213217 000
06934415011150 K213217 000
06934415011136 K213217 000
06934415012195 K213217 000
06934415012188 K213217 000
06934415011181 K213217 000

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