Model 980-Cardioscope At-3 Electrocardiograph

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K872658 ↗

FDA Product Code

DPS

Device Class

Class II

Regulation

21 CFR Part 870.2340

Advisory Committee

Cardiovascular

FDA Decision

SESE Substantially Equivalent

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  FDA 510(k) K850044 Active Cleared 4 Apr 1985

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