Class Class II

Tristel Duo ULT (DEN220041)

DEN220041 2023-06-02 Direct
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Description

Tristel Duo ULT by Tristel Solutions Limited — FDA 510(k) cleared general hospital device.

Regulatory Information

Device ClassClass Class II
510(k) NumberDEN220041
Clearance Date2023-06-02
Clearance TypeDirect
Product CodeQWS
Regulation Number880.6886

Categories

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