Models 43100A, 43110A & 43120A Defibrillator/Monit

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K844740 ↗

FDA Product Code

LDD

Models / Variants

43100A

43110A

43120A Defibrillator

Monit

Device Class

Class II

Regulation

21 CFR Part 870.5300

Advisory Committee

Cardiovascular

FDA Decision

SESE Substantially Equivalent

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