Cleared Traditional

K830843 - BLOOD GAS SOLUTIONS & CO-OXIMETER SOLU- (FDA 510(k) Clearance)

Class I Chemistry device.

K830843 · Rna Medical Corp. · Chemistry device
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Apr 1983
Decision
42d
Days
Class 1
Risk

K830843 is an FDA 510(k) clearance for the BLOOD GAS SOLUTIONS & CO-OXIMETER SOLU-. Classified as Gas Chromatograph, Carbon-monoxide (product code JKT), Class I - General Controls.

Submitted by Rna Medical Corp. (Mchenry, US). The FDA issued a Cleared decision on April 28, 1983 after a review of 42 days - a notably fast clearance cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.3220 - 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 Rna Medical Corp. devices

Submission Details

510(k) Number K830843 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 17, 1983
Decision Date April 28, 1983
Days to Decision 42 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
46d faster than avg
Panel avg: 88d · This submission: 42d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code JKT Gas Chromatograph, Carbon-monoxide
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 862.3220
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.