Gen. Diag. Chromostrate Plasminogen Assay

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

510(k) Number

K850410 ↗

FDA Product Code

DDX

Device Class

Class I

Regulation

21 CFR Part 866.5715

Advisory Committee

Immunology

FDA Decision

SESE Substantially Equivalent

• General Diagnostics Coag-a-Mate Xc

  Class I

  FDA 510(k) K852843 Active Cleared 13 Aug 1985

• Chick Surgical Table

  Class I

  FDA 510(k) K800118 Active Cleared 5 Feb 1980

• A O Microscope Video System

  Class I

  FDA 510(k) K821865 Active Cleared 14 Jul 1982

• Deseret Angio Guide

  Class II

  FDA 510(k) K821577 Active Cleared 16 Jun 1982

• A O Histostat Embedding Ctr #8030, 32, 34

  Class I

  FDA 510(k) K821831 Active Cleared 13 Jul 1982

• Deseret Capacity Plus Electrosurg. Pad

  Class II

  FDA 510(k) K821356 Active Cleared 14 Jul 1982

See all devices from Warner-Lambert Co. →