Cleared Traditional

HARRIS HEMATOXYLIN, MERCURY FREE, ACID

K843425 · Accra Laboratories, Inc. · Pathology
Oct 1984
Decision
28d
Days
Class 1
Risk

About This 510(k) Submission

K843425 is an FDA 510(k) clearance for the HARRIS HEMATOXYLIN, MERCURY FREE, ACID, a Hematoxylin Harris's (Class I — General Controls, product code HYK), submitted by Accra Laboratories, Inc. (Mchenry, US). The FDA issued a Cleared decision on October 2, 1984, 28 days after receiving the submission on September 4, 1984. This device falls under the Pathology review panel. Regulated under 21 CFR 864.1850.

Submission Details

510(k) Number K843425 FDA.gov
FDA Decision Cleared SESE
Date Received September 04, 1984
Decision Date October 02, 1984
Days to Decision 28 days
Submission Type Traditional
Review Panel Pathology (PA)
Summary

Device Classification

Product Code HYK — Hematoxylin Harris's
Device Class Class I — General Controls
CFR Regulation 21 CFR 864.1850