Cleared Traditional

K874031 - IRMA-COUNT FERRITIN W/MONO. ANTIBODIES ...

K874031 is the FDA 510(k) clearance for IRMA-COUNT FERRITIN W/MONO. ANTIBODIES ... by Diagnostic Products Corp.. It is a Class 2 Immunology device (product code DBF) cleared through the Traditional 510(k) pathway after a 54-day FDA review.

K874031 · Diagnostic Products Corp. · Immunology device
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Nov 1987
Decision
54d
Days
Class 2
Risk

K874031 is an FDA 510(k) clearance for the IRMA-COUNT FERRITIN W/MONO. ANTIBODIES RKFE1,2,5. Classified as Ferritin, Antigen, Antiserum, Control (product code DBF), Class II - Special Controls.

Submitted by Diagnostic Products Corp. (Los Angeles, US). The FDA issued a Cleared decision on November 25, 1987 after a review of 54 days - a notably fast clearance cycle.

This device falls under the Immunology FDA review panel, regulated under 21 CFR 866.5340 - the FDA immunology 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 Diagnostic Products Corp. devices

Submission Details

510(k) Number K874031 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 02, 1987
Decision Date November 25, 1987
Days to Decision 54 days
Submission Type Traditional
Review Panel Immunology (IM)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
50d faster than avg
Panel avg: 104d · This submission: 54d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code DBF Ferritin, Antigen, Antiserum, Control
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 866.5340
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 Immunology devices follow this clearance model.

Regulatory Peers - DBF Ferritin, Antigen, Antiserum, Control

All 51
Devices cleared under the same product code (DBF) and FDA review panel - the closest regulatory comparables to K874031.
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K870570 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Mar 1987