Cleared Traditional

K992517 - BIOCHECK FERRITIN ELISA MODEL BC-1025

K992517 is an FDA 510(k) clearance for BIOCHECK FERRITIN ELISA MODEL BC-1025, manufactured by Biocheck, Inc.. The device is a Class 2 Immunology device with product code DBF cleared through the Traditional 510(k) pathway after a 58-day FDA review.

K992517 · Biocheck, Inc. · Immunology device
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Sep 1999
Decision
58d
Days
Class 2
Risk

K992517 is an FDA 510(k) clearance for the BIOCHECK FERRITIN ELISA MODEL BC-1025. Classified as Ferritin, Antigen, Antiserum, Control (product code DBF), Class II - Special Controls.

Submitted by Biocheck, Inc. (Northridge, US). The FDA issued a Cleared decision on September 24, 1999 after a review of 58 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 Biocheck, Inc. devices

FDA 510(k) Submission Details - K992517

510(k) Number K992517 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 28, 1999
Decision Date September 24, 1999
Days to Decision 58 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
47d faster than avg
Panel avg: 105d · This submission: 58d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DBF Device Classification - Class 2, Special Controls

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 72
Devices cleared under the same product code (DBF) and FDA review panel - the closest regulatory comparables to K992517.
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NICHOLS ADVANTAGE CHEMILUMINESCENCE FERRITIN IMMUNOASSAY
K984186 · Nichols Institute Diagnostics · Feb 1999
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K983340 · Beckman Coulter, Inc. · Dec 1998