Storz Aspiration Machine Sam 5000

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K843644 ↗

FDA Product Code

BTA

Device Class

Class II

Regulation

21 CFR Part 878.4780

Advisory Committee

General, Plastic Surgery

FDA Decision

SESE Substantially Equivalent

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  Class II

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• Storz Premiere/Premiere Microvit Microsurg Systems

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  FDA 510(k) K921460 Active Cleared 2 Jul 1992

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