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510(k) FDA Premarket Notification K221839

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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
16950383616361 K221839 000
16950383616231 K221839 000
16950383616224 K221839 000
16950383616217 K221839 000
16950383616200 K221839 000
16950383616194 K221839 000
16950383616187 K221839 000
16950383616170 K221839 000
16950383616163 K221839 000
16950383616156 K221839 000
16950383616149 K221839 000
16950383616248 K221839 000
16950383616255 K221839 000
16950383616354 K221839 000
16950383616347 K221839 000
16950383616330 K221839 000
16950383616323 K221839 000
16950383616316 K221839 000
16950383616309 K221839 000
16950383616293 K221839 000
16950383616286 K221839 000
16950383616279 K221839 000
16950383616262 K221839 000
86950383616131 K221839 000

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