Cleared Traditional

K850999 - TECHNICON GEN 2 SYS & ANALYTES LD

K850999 is the FDA 510(k) clearance for TECHNICON GEN 2 SYS & ANALYTES LD by Technicon Instruments Corp.. It is a Class 1 Chemistry device (product code JJF) cleared through the Traditional 510(k) pathway after a 28-day FDA review.

K850999 · Technicon Instruments Corp. · Chemistry device
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Apr 1985
Decision
28d
Days
Class 1
Risk

K850999 is an FDA 510(k) clearance for the TECHNICON GEN 2 SYS & ANALYTES LD, ALP CK, UN, IN. Classified as Analyzer, Chemistry, Micro, For Clinical Use (product code JJF), Class I - General Controls.

Submitted by Technicon Instruments Corp. (Tarrytown, US). The FDA issued a Cleared decision on April 8, 1985 after a review of 28 days - a notably fast clearance cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.2170 - the FDA in vitro diagnostics and chemistry 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 Technicon Instruments Corp. devices

Submission Details

510(k) Number K850999 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 11, 1985
Decision Date April 08, 1985
Days to Decision 28 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
60d faster than avg
Panel avg: 88d · This submission: 28d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code JJF Analyzer, Chemistry, Micro, For Clinical Use
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 862.2170
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.

Regulatory Peers - JJF Analyzer, Chemistry, Micro, For Clinical Use

All 32
Devices cleared under the same product code (JJF) and FDA review panel - the closest regulatory comparables to K850999.
SYNCHRON CX3
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K833998 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Jan 1984
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K833804 · Shaban Mfg. Co. · Jan 1984