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510(k) FDA Premarket Notification P110004

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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
07290107010757 P110004 001
07290107010917 P110004 001
07290107010900 P110004 001
07290107010894 P110004 001
07290107010887 P110004 001
07290107010870 P110004 001
07290107010863 P110004 001
07290107010856 P110004 001
07290107010849 P110004 001
07290107010832 P110004 001
07290107010825 P110004 001
07290107010818 P110004 001
07290107010801 P110004 001
07290107010795 P110004 001
07290107010788 P110004 001
07290107010771 P110004 001
07290107010764 P110004 001
07290107010924 P110004 001
07290107010931 P110004 001
07290107010948 P110004 001
07290107011068 P110004 001
07290107011051 P110004 001
07290107011044 P110004 001
07290107011037 P110004 001
07290107011020 P110004 001
07290107011013 P110004 001
07290107011006 P110004 001
07290107010955 P110004 001
07290107010962 P110004 001
07290107010979 P110004 001
07290107010986 P110004 001
07290107010993 P110004 001
07290107012942 P110004 018
07290107012959 P110004 018
07290107012966 P110004 018
07290107012973 P110004 018
07290107012980 P110004 018

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