Cleared Traditional

K872500 - ANATECH HEMATOXYLIN-EXTRA STRENGTH (FDA 510(k) Clearance)

Class I Pathology device.

K872500 · Anatech, Ltd. · Pathology device
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Jul 1987
Decision
15d
Days
Class 1
Risk

K872500 is an FDA 510(k) clearance for the ANATECH HEMATOXYLIN-EXTRA STRENGTH. Classified as Hematoxylin (product code HYJ), Class I - General Controls.

Submitted by Anatech, Ltd. (Battle Creek, US). The FDA issued a Cleared decision on July 9, 1987 after a review of 15 days - a notably fast clearance cycle.

This device falls under the Pathology FDA review panel, regulated under 21 CFR 864.1850 - the FDA pathology device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Anatech, Ltd. devices

Submission Details

510(k) Number K872500 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 24, 1987
Decision Date July 09, 1987
Days to Decision 15 days
Submission Type Traditional
Review Panel Pathology (PA)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
62d faster than avg
Panel avg: 77d · This submission: 15d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code HYJ Hematoxylin
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 864.1850
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.