Pneumocystis Carinii Immunofluorescence Test Kit

No FDA recalls found in the data synced 11 Oct 2026.

510(k) Number

K890768 ↗

FDA Product Code

LYF

Device Class

Class II

Regulation

21 CFR Part 866.3780

Advisory Committee

Microbiology

FDA Decision

SESE Substantially Equivalent

• Genetic Systems Rsv Reagent Control Slides

  Class I

  FDA 510(k) K873564 Active Cleared 20 Nov 1987

• Genetic Systems Rsv Immunofluorescence Test Kit

  Class I

  FDA 510(k) K870176 Active Cleared 16 Jul 1987

• Microplate Auto-Washer (Motorized Stage)

  Class I

  FDA 510(k) K873542 Active Cleared 23 Sep 1987

• Legionella Immunofluorescent Antibody Test Kit

  Class II

  FDA 510(k) K852237 Active Cleared 22 Aug 1985

• Genetic Systems Pipettor/Dilutor

  Class I

  FDA 510(k) K891765 Active Cleared 1 May 1989

• Genetic Systems Microplate Washer

  Class I

  FDA 510(k) K891768 Active Cleared 1 May 1989

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