Cleared Traditional

K790059 - PROACTIVATOR C3, C4 AND C3

K790059 is an FDA 510(k) clearance for PROACTIVATOR C3, manufactured by Icl Scientific. The device is a Class 2 Immunology device with product code KTP cleared through the Traditional 510(k) pathway after a 65-day FDA review.

K790059 · Icl Scientific · Immunology device
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Mar 1979
Decision
65d
Days
Class 2
Risk

K790059 is an FDA 510(k) clearance for the PROACTIVATOR C3, C4 AND C3. Classified as Complement C3b Activator Immunoassay Reagents (product code KTP), Class II - Special Controls.

Submitted by Icl Scientific (Mchenry, US). The FDA issued a Cleared decision on March 15, 1979 after a review of 65 days - a notably fast clearance cycle.

This device falls under the Immunology FDA review panel, regulated under 21 CFR 866.5260 - 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 Icl Scientific devices

FDA 510(k) Submission Details - K790059

510(k) Number K790059 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 09, 1979
Decision Date March 15, 1979
Days to Decision 65 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
40d faster than avg
Panel avg: 105d · This submission: 65d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

KTP Device Classification - Class 2, Special Controls

Product Code KTP Complement C3b Activator Immunoassay Reagents
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 866.5260
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.