Microlite Microtiter Plate Luminometer ML3000

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K923456 ↗

FDA Product Code

JJQ

Device Class

Class I

Regulation

21 CFR Part 862.2300

Advisory Committee

Clinical Chemistry

FDA Decision

SESE Substantially Equivalent

• Microlite Ml 1000 Microtiter Plate Luminometer

  Class I

  FDA 510(k) K913590 Active Cleared 25 Oct 1991

• Histo-Dispenser

  Class I

  FDA 510(k) K790957 Active Cleared 15 Jun 1979

• Cell

  Class I

  FDA 510(k) K780305 Active Cleared 27 Mar 1978

• Mr 700 Microplate Reader 012-700-1000

  Class I

  FDA 510(k) K854303 Active Cleared 19 Nov 1985

• Mic-2000 Quad Inoculum Tray

  Class I

  FDA 510(k) K790971 Active Cleared 20 Jun 1979

• Dynatech Mr 300 Manual Microelisa

  Class I

  FDA 510(k) K874244 Active Cleared 3 Nov 1987

See all devices from Dynatech Laboratories, Inc. →