Cleared Traditional

HA/3 HEMATOLOGY ANALYZER (K760582) - FDA 510(k) Clearance

Class II Hematology device cleared through predicate-based substantial equivalence - typically does not require clinical trials.

K760582 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Hematology device
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Nov 1976
Decision
69d
Days
Class 2
Risk

K760582 is an FDA 510(k) clearance for the HA/3 HEMATOLOGY ANALYZER. Classified as Counter, Cell, Automated (particle Counter) (product code GKL), Class II - Special Controls.

Submitted by Bd Becton Dickinson Vacutainer Systems Preanalytic (Washington, US). The FDA issued a Cleared decision on November 11, 1976 after a review of 69 days - a notably fast clearance cycle.

This device falls under the Hematology FDA review panel, regulated under 21 CFR 864.5200 - 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 Bd Becton Dickinson Vacutainer Systems Preanalytic devices

Submission Details

510(k) Number K760582 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 03, 1976
Decision Date November 11, 1976
Days to Decision 69 days
Submission Type Traditional
Review Panel Hematology (HE)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
44d faster than avg
Panel avg: 113d · This submission: 69d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code GKL Counter, Cell, Automated (particle Counter)
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 864.5200
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 - GKL Counter, Cell, Automated (particle Counter)

All 23
Devices cleared under the same product code (GKL) and FDA review panel - the closest regulatory comparables to K760582.
HEMALOG 8/90
K770666 · Technicon Instruments Corp. · May 1977
LATELET DETERMIN. KIT, CAT NO. 2521
K770385 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Apr 1977
ULTRA LOGIC 800 HEMATOLOGY ANA. (UL-800)
K761289 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Mar 1977
HA/5 HEMATOLOGY ANALYZER
K760581 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Nov 1976