Cleared Traditional

K813127 - SODIUM & POTASSIUM PRODUCTS

K813127 is the FDA 510(k) clearance for SODIUM & POTASSIUM PRODUCTS by Alko Diagnostic Corp.. It is a Class 2 Chemistry device (product code JIX) cleared through the Traditional 510(k) pathway after a 78-day FDA review.

K813127 · Alko Diagnostic Corp. · Chemistry device
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Jan 1982
Decision
78d
Days
Class 2
Risk

K813127 is an FDA 510(k) clearance for the SODIUM & POTASSIUM PRODUCTS. Classified as Calibrator, Multi-analyte Mixture (product code JIX), Class II - Special Controls.

Submitted by Alko Diagnostic Corp. (Mchenry, US). The FDA issued a Cleared decision on January 22, 1982 after a review of 78 days - a notably fast clearance cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1150 - 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 Alko Diagnostic Corp. devices

Submission Details

510(k) Number K813127 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 05, 1981
Decision Date January 22, 1982
Days to Decision 78 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
10d faster than avg
Panel avg: 88d · This submission: 78d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code JIX Calibrator, Multi-analyte Mixture
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.1150
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 - JIX Calibrator, Multi-analyte Mixture

All 202
Devices cleared under the same product code (JIX) and FDA review panel - the closest regulatory comparables to K813127.
NOVA III FLUIDS PACK
K820947 · Shaban Mfg. Co. · Apr 1982
EXTERNAL STANDARDS-SODIUMNPOTASSIUM
K820700 · Shaban Mfg. Co. · Apr 1982
NOVA I FLUIDS PACK
K820701 · Shaban Mfg. Co. · Apr 1982
BECKMAN ICS CALIBRATOR
K812649 · Beckman Instruments, Inc. · Oct 1981
HITACHI 705 CALIBRATOR
K811921 · Boehringer Mannheim Corp. · Jul 1981
BIO SET TM PHOSPHOROUS CALIBRATOR
K810964 · Boehringer Mannheim Corp. · Apr 1981