Cleared Traditional

K790653 - NOVA 3 CHLORIDE/TOTAL DIOXIDE ANALYZER

K790653 is an FDA 510(k) clearance for NOVA 3 CHLORIDE/TOTAL DIOXIDE ANALYZER, manufactured by Nova Corp.. The device is a Class 2 Chemistry device with product code CGZ cleared through the Traditional 510(k) pathway after a 71-day FDA review.

K790653 · Nova Corp. · Chemistry device
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Jun 1979
Decision
71d
Days
Class 2
Risk

K790653 is an FDA 510(k) clearance for the NOVA 3 CHLORIDE/TOTAL DIOXIDE ANALYZER. Classified as Electrode, Ion-specific, Chloride (product code CGZ), Class II - Special Controls.

Submitted by Nova Corp. (Mchenry, US). The FDA issued a Cleared decision on June 15, 1979 after a review of 71 days - a notably fast clearance cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1170 - 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 Nova Corp. devices

FDA 510(k) Submission Details - K790653

510(k) Number K790653 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 05, 1979
Decision Date June 15, 1979
Days to Decision 71 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
17d faster than avg
Panel avg: 88d · This submission: 71d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

CGZ Device Classification - Class 2, Special Controls

Product Code CGZ Electrode, Ion-specific, Chloride
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.1170
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.