Cleared Traditional

K875102 - DETER. OF HEMOGLOBIN A2 USING THE DIAMAT

K875102 is the FDA 510(k) clearance for DETER. OF HEMOGLOBIN A2 USING THE DIAMAT by Bio-Rad. It is a Class 2 Hematology device (product code JPD) cleared through the Traditional 510(k) pathway after a 76-day FDA review.

K875102 · Bio-Rad · Hematology device
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Feb 1988
Decision
76d
Days
Class 2
Risk

K875102 is an FDA 510(k) clearance for the DETER. OF HEMOGLOBIN A2 USING THE DIAMAT. Classified as Hemoglobin A2 Quantitation (product code JPD), Class II - Special Controls.

Submitted by Bio-Rad (Hercules, US). The FDA issued a Cleared decision on February 24, 1988 after a review of 76 days - a notably fast clearance cycle.

This device falls under the Hematology FDA review panel, regulated under 21 CFR 864.7400 - 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 K875102 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 10, 1987
Decision Date February 24, 1988
Days to Decision 76 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
37d faster than avg
Panel avg: 113d · This submission: 76d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code JPD Hemoglobin A2 Quantitation
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 864.7400
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 - JPD Hemoglobin A2 Quantitation

All 11
Devices cleared under the same product code (JPD) and FDA review panel - the closest regulatory comparables to K875102.
COLUMNMATE BETA-THAL HBA2 CONTROL - NORMAL
K923318 · Helena Laboratories · Aug 1992
COLUMNMATE(TM) BETA-THAL CAT. NO. 4515
K913384 · Helena Laboratories · Dec 1991
HEMOGLOBIN A2 MICRO COLUMN TEST
K896168 · Bio-Rad · Jan 1990
BETA THALQUIK COLUMN #5341
K823870 · Helena Laboratories · Feb 1983
HELENA SICKLE-THAL QUIK COLUMN METHOD
K812077 · Helena Laboratories · Aug 1981
HELENA HBA2 QUIK COLUMN METHOD
K803108 · Helena Laboratories · Jan 1981