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510(k) FDA Premarket Notification K232414

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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
00814703019289 K232414 000
00814703019098 K232414 000
00814703019081 K232414 000
00814703019074 K232414 000
00814703019067 K232414 000
00814703019050 K232414 000
00814703016622 K232414 000
00814703016554 K232414 000
00814703016486 K232414 000
00814703016417 K232414 000
00814703016349 K232414 000
00814703016271 K232414 000
00814703016202 K232414 000
00814703016134 K232414 000
00814703016066 K232414 000
00814703015991 K232414 000
00814703015922 K232414 000
00814703019104 K232414 000
00814703019111 K232414 000
00814703019272 K232414 000
00814703019265 K232414 000
00814703019258 K232414 000
00814703019241 K232414 000
00814703019234 K232414 000
00814703019227 K232414 000
00814703019210 K232414 000
00814703019203 K232414 000
00814703019197 K232414 000
00814703019180 K232414 000
00814703019173 K232414 000
00814703019166 K232414 000
00814703019159 K232414 000
00814703019142 K232414 000
00814703019135 K232414 000
00814703019128 K232414 000
00814703015854 K232414 000

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