Cleared Traditional

K833072 - TECHNICON RA-1000 SYS-ISE MODULE &

K833072 is the FDA 510(k) clearance for TECHNICON RA-1000 SYS-ISE MODULE & by Technicon Instruments Corp.. It is a Class 2 Chemistry device (product code JGS) cleared through the Traditional 510(k) pathway after a 67-day FDA review.

K833072 · Technicon Instruments Corp. · Chemistry device
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Nov 1983
Decision
67d
Days
Class 2
Risk

K833072 is an FDA 510(k) clearance for the TECHNICON RA-1000 SYS-ISE MODULE &. Classified as Electrode, Ion Specific, Sodium (product code JGS), Class II - Special Controls.

Submitted by Technicon Instruments Corp. (Walker, US). The FDA issued a Cleared decision on November 14, 1983 after a review of 67 days - a notably fast clearance cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1665 - 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 K833072 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 08, 1983
Decision Date November 14, 1983
Days to Decision 67 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
21d faster than avg
Panel avg: 88d · This submission: 67d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code JGS Electrode, Ion Specific, Sodium
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.1665
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 Chemistry devices follow this clearance model.

Regulatory Peers - JGS Electrode, Ion Specific, Sodium

All 111
Devices cleared under the same product code (JGS) and FDA review panel - the closest regulatory comparables to K833072.
REAGENTS & STANDARDS IL 501 NA/K
K840557 · Shaban Mfg. Co. · Apr 1984
TECHNICON RA-1000 SYSTEM
K833992 · Technicon Instruments Corp. · Jan 1984
NA/K FLUIDA PACK FOR NOVA 1 ANALYZER
K833712 · Fisher Scientific Co., LLC · Jan 1984
FLOW-PAC SODIUM REAGENT SET
K833036 · American Research Products Co. · Nov 1983
STARLYTE
K832744 · Electro-Nucleonics Laboratories, Inc. · Nov 1983
DEPROTEINIZING & CLEANING SOLUTION
K832415 · Shaban Mfg. Co. · Sep 1983