Cleared Traditional

K901805 - REP IMMUNOFIX

K901805 is the FDA 510(k) clearance for REP IMMUNOFIX by Helena Laboratories. It is a Class 2 Immunology device (product code DAH) cleared through the Traditional 510(k) pathway after a 47-day FDA review.

K901805 · Helena Laboratories · Immunology device
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Jun 1990
Decision
47d
Days
Class 2
Risk

K901805 is an FDA 510(k) clearance for the REP(R) IMMUNOFIX. Classified as Gamma Globulin, Antigen, Antiserum, Control (product code DAH), Class II - Special Controls.

Submitted by Helena Laboratories (Beaumont, US). The FDA issued a Cleared decision on June 6, 1990 after a review of 47 days - a notably fast clearance cycle.

This device falls under the Immunology FDA review panel, regulated under 21 CFR 866.5510 - 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 Helena Laboratories devices

Submission Details

510(k) Number K901805 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 20, 1990
Decision Date June 06, 1990
Days to Decision 47 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
57d faster than avg
Panel avg: 104d · This submission: 47d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code DAH Gamma Globulin, Antigen, Antiserum, Control
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 866.5510
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 - DAH Gamma Globulin, Antigen, Antiserum, Control

Devices cleared under the same product code (DAH) and FDA review panel - the closest regulatory comparables to K901805.
TITAN GEL IMMUNOFIX-9 CAT. NO. 3051 AND 3067
K931247 · Helena Laboratories · Apr 1993
TITAN GEL
K905149 · Helena Laboratories · Jan 1991
TECHNICON DPA-1 IMMUNOGLOBULIN G
K883494 · Technicon Instruments Corp. · Sep 1988
TDX IMMUNOGLOBULIN M DIAGNOSTIC KIT
K854944 · Abbott Laboratories · Aug 1986
DAKO ITA, IMMUNOGLOBULIN M (IGM)
K862184 · Dako Corp. · Aug 1986