Provial Ii #006-010-0201

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K823773 ↗

FDA Product Code

KDT

Device Class

Class I

Regulation

21 CFR Part 864.3250

Advisory Committee

Pathology

FDA Decision

SESE Substantially Equivalent

• Mini-Shaker

  Class I

  FDA 510(k) K813318 Active Cleared 17 Dec 1981

• 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

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