Procainamide Analytical Test Pack

No FDA recalls found in the data synced 10 Oct 2026.

510(k) Number

K833384 ↗

FDA Product Code

LAR

Device Class

Class II

Regulation

21 CFR Part 862.3320

Advisory Committee

Clinical Toxicology

FDA Decision

SESE Substantially Equivalent

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See all devices from E.I. Dupont DE Nemours & Co., Inc. →