Cleared Traditional

K854079 - THROMBO SCREEN SICKLE CELL ASSAY SET

K854079 is the FDA 510(k) clearance for THROMBO SCREEN SICKLE CELL ASSAY SET by Pacific Hemostasis. It is a Class 2 Hematology device (product code GHM) cleared through the Traditional 510(k) pathway after a 24-day FDA review.

K854079 · Pacific Hemostasis · Hematology device
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Oct 1985
Decision
24d
Days
Class 2
Risk

K854079 is an FDA 510(k) clearance for the THROMBO SCREEN SICKLE CELL ASSAY SET. Classified as Test, Sickle Cell (product code GHM), Class II - Special Controls.

Submitted by Pacific Hemostasis (Ventura, US). The FDA issued a Cleared decision on October 31, 1985 after a review of 24 days - a notably fast clearance cycle.

This device falls under the Hematology FDA review panel, regulated under 21 CFR 864.7825 - the FDA hematology 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 Pacific Hemostasis devices

Submission Details

510(k) Number K854079 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 07, 1985
Decision Date October 31, 1985
Days to Decision 24 days
Submission Type Traditional
Review Panel Hematology (HE)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
89d faster than avg
Panel avg: 113d · This submission: 24d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code GHM Test, Sickle Cell
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 864.7825
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Hematology devices follow this clearance model.

Regulatory Peers - GHM Test, Sickle Cell

All 9
Devices cleared under the same product code (GHM) and FDA review panel - the closest regulatory comparables to K854079.
HEMOCARD HEMOGLOBIN S
K911981 · Isolab, Inc. · Oct 1991
HEMOCARD-AS
K910430 · Isolab, Inc. · Apr 1991
SICKLE CELL REAGENT SET
K860420 · Sterling Diagnostics, Inc. · Feb 1986
SICKLING HEMOGLOBIN CONTROLS, NORMAL
K842152 · Isolab, Inc. · Sep 1984
SICKLE HB ASSAY
K841170 · Isolab, Inc. · Apr 1984
MONOJECT SICKLE CELL KIT
K791971 · Sherwood Medical Co. · Nov 1979