Erythocyte Creatine

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K852767 ↗

FDA Product Code

JLA

Device Class

Class I

Regulation

21 CFR Part 862.1210

Advisory Committee

Clinical Chemistry

FDA Decision

SESE Substantially Equivalent

• Sickle-Check

  Class II

  FDA 510(k) K820642 Active Cleared 14 Apr 1982

• Postassium Buffer Sol. & Wash Solution

  Class II

  FDA 510(k) K802158 Active Cleared 10 Oct 1980

• Alfatest

  Class I

  FDA 510(k) K780542 Active Cleared 19 May 1978

• Bun Color Reagent & Bun Acid Used

  Class II

  FDA 510(k) K802160 Active Cleared 10 Oct 1980

• Reagents Used-Quan. Measure of Serum

  Class II

  FDA 510(k) K802154 Active Cleared 10 Oct 1980

• 8-Hydroxyquinoline, Cresolphthalein Com.

  Class II

  FDA 510(k) K802164 Active Cleared 10 Oct 1980

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