Mini-Shaker

No FDA recalls on record, checked 10 Oct 2026.

510(k) Number

K813318 ↗

FDA Product Code

JRQ

Device Class

Class I

Regulation

21 CFR Part 862.2050

Advisory Committee

Clinical Chemistry

FDA Decision

SESE Substantially Equivalent

• Microerma System

  Class I

  FDA 510(k) K811001 Active Cleared 1 May 1981

• Microfluor B Plate & Micro Fluor W Plate

  Class I

  FDA 510(k) K822960 Active Cleared 16 Nov 1982

• Auto Mash

  Class I

  FDA 510(k) K854604 Active Cleared 6 Dec 1985

• Replica Plater

  Class I

  FDA 510(k) K810719 Active Cleared 1 Apr 1981

• Multi Mash 2000

  Class I

  FDA 510(k) K854603 Active Cleared 6 Dec 1985

• Dynatech MR4000 Microplate Reader

  Class I

  FDA 510(k) K904567 Active Cleared 28 Jan 1991

See all devices from Dynatech Corp. →