Cardiopac Defibrillator 444

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K844103 ↗

FDA Product Code

LDD

Device Class

Class II

Regulation

21 CFR Part 870.5300

Advisory Committee

Cardiovascular

FDA Decision

SESE Substantially Equivalent

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• Surgical Cauteries Models 775-11, 12, 13, 31, 32 & 33

  Class II

  FDA 510(k) K854814 Active Cleared 13 Jan 1986

See all devices from Birtcher Corp. →