Satari Latex Patient Examination Powdered Glove Single Side Polymer Coated, Non Sterile, 200 Mg or Less of Total Water E

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K014112 ↗

FDA Product Code

LYY

Device Class

Class I

Regulation

21 CFR Part 880.6250

Advisory Committee

General Hospital

FDA Decision

SESE Substantially Equivalent

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