Aca(R) C-Reactive Protein (Crp) Analytical Test

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K863328 ↗

FDA Product Code

DCK

Device Class

Class II

Regulation

21 CFR Part 866.5270

Advisory Committee

Immunology

FDA Decision

SESE Substantially Equivalent

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