Cleared Traditional

K003030 - LYPHOCHEK HEMOGLOBIN ALC LINEARITY SET

K003030 is the FDA 510(k) clearance for LYPHOCHEK HEMOGLOBIN ALC LINEARITY SET by Bio-Rad. It is a Class 2 Hematology device (product code GGM) cleared through the Traditional 510(k) pathway after a 62-day FDA review.

K003030 · Bio-Rad · Hematology device
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Nov 2000
Decision
62d
Days
Class 2
Risk

K003030 is an FDA 510(k) clearance for the LYPHOCHEK HEMOGLOBIN ALC LINEARITY SET. Classified as Control, Hemoglobin (product code GGM), Class II - Special Controls.

Submitted by Bio-Rad (Irvine, US). The FDA issued a Cleared decision on November 29, 2000 after a review of 62 days - a notably fast clearance cycle.

This device falls under the Hematology FDA review panel, regulated under 21 CFR 864.8625 - 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 Bio-Rad devices

Submission Details

510(k) Number K003030 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 28, 2000
Decision Date November 29, 2000
Days to Decision 62 days
Submission Type Traditional
Review Panel Hematology (HE)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
51d faster than avg
Panel avg: 113d · This submission: 62d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code GGM Control, Hemoglobin
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 864.8625
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 - GGM Control, Hemoglobin

All 11
Devices cleared under the same product code (GGM) and FDA review panel - the closest regulatory comparables to K003030.
R&D SICKLE QC CONTROL
K070334 · R&D Systems, Inc. · Mar 2007
LIQUICHEK DIABETES CONTROL, LEVEL 1,2,3,4
K052838 · Bio-Rad · Nov 2005
GLYCOHEMOSURE HBA1C CONTROL
K032791 · Quantimetrix Corp. · Oct 2003
R&D HGB/GLC WHOLE BLOOD CONTROL
K993321 · R&D Systems, Inc. · Nov 1999
CRITERION, HEMOCUE B-HEMOGLOBIN CONTROL
K921681 · Isolab, Inc. · Nov 1992
HGB-CONTROL SET/MULTIPLE
K893985 · R&D Systems, Inc. · Aug 1989