Storz Millennium Viscous Fluid System

No FDA recalls on record, checked 10 Oct 2026.

510(k) Number

K972664 ↗

FDA Product Code

MRH

Device Class

Class II

Regulation

21 CFR Part 880.5725

Advisory Committee

General Hospital

FDA Decision

SESE Substantially Equivalent

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• Storz Premiere/Premiere Microvit Microsurg Systems

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