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510(k) FDA Premarket Notification P890055

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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
10886704043591 P890055 001
10886704043607 P890055 001
10886704043614 P890055 001
10886704043621 P890055 001
10886704072553 P890055 005
10886704043775 P890055 010
10886704078838 P890055 010
20886704043741 P890055 010
20886704043727 P890055 010
10886704043768 P890055 011
20886704043826 P890055 012
10886704043751 P890055 016
10886704034995 P890055 018
10886704072560 P890055 018
20886704043710 P890055 021
20886704072888 P890055 021
20886704043734 P890055 021
20886704071454 P890055 026
10886704064923 P890055 026
10886704064930 P890055 026
10886704071433 P890055 026
20886704064951 P890055 031
10886704072072 P890055 031
10850014110021 P890055 073
00850014110079 P890055 073
10850014110045 P890055 073
10850014110052 P890055 073
00850014110147 P890055 074
00850014110154 P890055 076
00850014110093 P890055 077

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