Cleared Traditional

K811400 - HEMAQUIK

K811400 is an FDA 510(k) clearance for HEMAQUIK, manufactured by Accra Laboratories, Inc.. The device is a Class 1 Pathology device with product code IAF cleared through the Traditional 510(k) pathway after a 31-day FDA review.

K811400 · Accra Laboratories, Inc. · Pathology device
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Jun 1981
Decision
31d
Days
Class 1
Risk

K811400 is an FDA 510(k) clearance for the HEMAQUIK. Classified as Wright's Stain (product code IAF), Class I - General Controls.

Submitted by Accra Laboratories, Inc. (Mchenry, US). The FDA issued a Cleared decision on June 18, 1981 after a review of 31 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 Accra Laboratories, Inc. devices

FDA 510(k) Submission Details - K811400

510(k) Number K811400 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 18, 1981
Decision Date June 18, 1981
Days to Decision 31 days
Submission Type Traditional
Review Panel Pathology (PA)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
46d faster than avg
Panel avg: 77d · This submission: 31d
Pathway characteristics
Predicate-based equivalence.

IAF Device Classification - Class 1, General Controls

Product Code IAF Wright's Stain
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.

Regulatory Peers - IAF Wright's Stain

All 18
Devices cleared under the same product code (IAF) and FDA review panel - the closest regulatory comparables to K811400.
AVES WRIGHT STAIN
K820437 · Helena Laboratories · Mar 1982
ACCRA LAB HEMOTOLOGY
K812848 · Accra Laboratories, Inc. · Oct 1981
ACCRA LAB WRIGHT STAIN
K812504 · Accra Laboratories, Inc. · Sep 1981
STAT STAIN SET
K810495 · Accra Laboratories, Inc. · Mar 1981
VOLU-SOL STATIM STAIN
K792497 · Volu Sol Medical Industries · Dec 1979
VOLU-SOL STAT STAIN
K792017 · Volu Sol Medical Industries · Oct 1979