Cleared Traditional

K000662 - RANDOX FERRITIN

K000662 is the FDA 510(k) clearance for RANDOX FERRITIN by Randox Laboratories, Ltd.. It is a Class 2 Immunology device (product code DBF) cleared through the Traditional 510(k) pathway after a 35-day FDA review.

K000662 · Randox Laboratories, Ltd. · Immunology device
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Apr 2000
Decision
35d
Days
Class 2
Risk

K000662 is an FDA 510(k) clearance for the RANDOX FERRITIN. Classified as Ferritin, Antigen, Antiserum, Control (product code DBF), Class II - Special Controls.

Submitted by Randox Laboratories, Ltd. (Crumlin, Co. Antrim, IE). The FDA issued a Cleared decision on April 3, 2000 after a review of 35 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 Randox Laboratories, Ltd. devices

Submission Details

510(k) Number K000662 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 28, 2000
Decision Date April 03, 2000
Days to Decision 35 days
Submission Type Traditional
Review Panel Immunology (IM)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
69d faster than avg
Panel avg: 104d · This submission: 35d
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 62
Devices cleared under the same product code (DBF) and FDA review panel - the closest regulatory comparables to K000662.
FERRITIN GENERATION 2
K031650 · Roche Diagnostics Corp. · Jul 2003
OLYMPUS FERRITIN REAGENT
K030124 · Olympus America, Inc. · Feb 2003
K-ASSAY FERRITIN, K-ASSAY FERRITIN CALIBRATOR SET
K014293 · Kamiya Biomedical Co. · Feb 2002
N LATEX FERRITIN
K993273 · Dade Behring, Inc. · Nov 1999
NICHOLS ADVANTAGE CHEMILUMINESCENCE FERRITIN IMMUNOASSAY
K984186 · Nichols Institute Diagnostics · Feb 1999
IMMAGE IMMUNOCHEMISTRY SYSTEM FERRITIN (FER)REAGENT, IMMAGE IMMUNOCHEMISTRY SYSTEM FERRITIN CALIBRATOR
K983340 · Beckman Coulter, Inc. · Dec 1998