Erythropoietin Immunoassay Kit

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

510(k) Number

K952559 ↗

FDA Product Code

GGT

Device Class

Class II

Regulation

21 CFR Part 864.7250

Advisory Committee

Hematology

FDA Decision

SESE Substantially Equivalent

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  Class II

  FDA 510(k) K930777 Active Cleared 8 Apr 1993

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  Class I

  FDA 510(k) K952505 Active Cleared 3 Jul 1995

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  FDA 510(k) K931777 Active Cleared 16 Aug 1993

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  FDA 510(k) K950524 Active Cleared 15 May 1995

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  Class II

  FDA 510(k) K931600 Active Cleared 8 Sep 1993

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