Cleared Traditional

K882767 - SYSMEX DD-100 WHOLE BLOOD DILUTION SYSTEM

K882767 is the FDA 510(k) clearance for SYSMEX DD-100 WHOLE BLOOD DILUTION SYSTEM by Toa Medical Electronics USA, Inc.. It is a Class 1 Hematology device (product code GKH) cleared through the Traditional 510(k) pathway after a 12-day FDA review.

K882767 · Toa Medical Electronics USA, Inc. · Hematology device
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Jul 1988
Decision
12d
Days
Class 1
Risk

K882767 is an FDA 510(k) clearance for the SYSMEX DD-100 WHOLE BLOOD DILUTION SYSTEM. Classified as Apparatus, Automated Blood Cell Diluting (product code GKH), Class I - General Controls.

Submitted by Toa Medical Electronics USA, Inc. (Los Alamitos, US). The FDA issued a Cleared decision on July 18, 1988 after a review of 12 days - a notably fast clearance cycle.

This device falls under the Hematology FDA review panel, regulated under 21 CFR 864.5240 - 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 Toa Medical Electronics USA, Inc. devices

Submission Details

510(k) Number K882767 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 06, 1988
Decision Date July 18, 1988
Days to Decision 12 days
Submission Type Traditional
Review Panel Hematology (HE)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
101d faster than avg
Panel avg: 113d · This submission: 12d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code GKH Apparatus, Automated Blood Cell Diluting
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 864.5240
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 - GKH Apparatus, Automated Blood Cell Diluting

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