Elisa Rubella Igm

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K914420 ↗

FDA Product Code

LFX

Device Class

Class II

Regulation

21 CFR Part 866.3510

Advisory Committee

Microbiology

FDA Decision

SESE Substantially Equivalent

• C-Reactive Protein Test Kit

  Class II

  FDA 510(k) K822332 Active Cleared 16 Aug 1982

• Isoenzyme Test Ck-Mb

  Class II

  FDA 510(k) K850212 Active Cleared 7 Feb 1985

• New Enzymatic Single Reagent Free Chol.

  Class I

  FDA 510(k) K822417 Active Cleared 21 Oct 1982

• Acp Kinetic Test (Acid Phosphatase Test)

  Class II

  FDA 510(k) K881204 Active Cleared 28 Apr 1988

• Diagnostic Kit, Cpk

  Class II

  FDA 510(k) K780311 Active Cleared 5 Apr 1978

• Total Iron Binding Capacity Test

  Class I

  FDA 510(k) K884649 Active Cleared 14 Dec 1988

See all devices from Sclavo, Inc. →