Esa Plasma Free Metanephrine Analysis Kit

No FDA recalls on record, checked 11 Oct 2026.

510(k) Number

K032199 ↗

FDA Product Code

CHQ

Device Class

Class I

Regulation

21 CFR Part 862.1165

Advisory Committee

Clinical Chemistry

FDA Decision

SESE Substantially Equivalent

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• Model 5500 Ceas

  Class I

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