Cleared Traditional

K882822 - FIAGEN FERRITIN

K882822 is an FDA 510(k) clearance for FIAGEN FERRITIN, manufactured by Cyberfluor, Inc.. The device is a Class 2 Immunology device with product code DFL cleared through the Traditional 510(k) pathway after a 27-day FDA review.

K882822 · Cyberfluor, Inc. · Immunology device
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Aug 1988
Decision
27d
Days
Class 2
Risk

K882822 is an FDA 510(k) clearance for the FIAGEN FERRITIN. Classified as Igm, Ferritin, Antigen, Antiserum, Control (product code DFL), Class II - Special Controls.

Submitted by Cyberfluor, Inc. (Ontario M5t 1x4, CA). The FDA issued a Cleared decision on August 4, 1988 after a review of 27 days - a notably fast clearance cycle.

This device falls under the Immunology FDA review panel, regulated under 21 CFR 866.5550 - 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 Cyberfluor, Inc. devices

FDA 510(k) Submission Details - K882822

510(k) Number K882822 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 08, 1988
Decision Date August 04, 1988
Days to Decision 27 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
78d faster than avg
Panel avg: 105d · This submission: 27d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DFL Device Classification - Class 2, Special Controls

Product Code DFL Igm, Ferritin, Antigen, Antiserum, Control
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 866.5550
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.