Cleared Traditional

DIA REPTIN (K841365) - FDA 510(k) Clearance

Class I Hematology device.

K841365 · Diatech, Inc. · Hematology device
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Jun 1984
Decision
60d
Days
Class 1
Risk

K841365 is an FDA 510(k) clearance for the DIA REPTIN. Classified as Reagent, Russel Viper Venom (product code GIR), Class I - General Controls.

Submitted by Diatech, Inc. (Mchenry, US). The FDA issued a Cleared decision on June 1, 1984 after a review of 60 days - a notably fast clearance cycle.

This device falls under the Hematology FDA review panel, regulated under 21 CFR 864.8950 - the FDA hematology 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 Diatech, Inc. devices

Submission Details

510(k) Number K841365 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 02, 1984
Decision Date June 01, 1984
Days to Decision 60 days
Submission Type Traditional
Review Panel Hematology (HE)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
53d faster than avg
Panel avg: 113d · This submission: 60d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code GIR Reagent, Russel Viper Venom
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 864.8950
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.