Appose Ultra Dispos. Skin Stapler W/Auto Release

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K844417 ↗

FDA Product Code

GAG

Device Class

Class II

Regulation

21 CFR Part 878.4740

Advisory Committee

General Hospital

FDA Decision

SESE Substantially Equivalent

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See all devices from Davis & Geck, Inc. →