Rmu-1000 Automated Chest Compression System

No FDA recalls on record, checked 10 Oct 2026.

510(k) Number

K141809 ↗

FDA Product Code

DRM

Device Class

Class II

Regulation

21 CFR Part 870.5200

Advisory Committee

Cardiovascular

FDA Decision

SESE Substantially Equivalent

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  FDA 510(k) K033144 Active Cleared 13 Nov 2003

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