Cleared Traditional

K792401 - ELVI INORGANIC PHOSPHOROUS

K792401 is an FDA 510(k) clearance for ELVI INORGANIC PHOSPHOROUS, manufactured by Volu Sol Medical Industries. The device is a Class 1 Chemistry device with product code CEO cleared through the Traditional 510(k) pathway after a 11-day FDA review.

K792401 · Volu Sol Medical Industries · Chemistry device
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Dec 1979
Decision
11d
Days
Class 1
Risk

K792401 is an FDA 510(k) clearance for the ELVI INORGANIC PHOSPHOROUS. Classified as Phosphomolybdate (colorimetric), Inorganic Phosphorus (product code CEO), Class I - General Controls.

Submitted by Volu Sol Medical Industries (Mchenry, US). The FDA issued a Cleared decision on December 7, 1979 after a review of 11 days - a notably fast clearance cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1580 - 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 Volu Sol Medical Industries devices

FDA 510(k) Submission Details - K792401

510(k) Number K792401 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 26, 1979
Decision Date December 07, 1979
Days to Decision 11 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
77d faster than avg
Panel avg: 88d · This submission: 11d
Pathway characteristics
Predicate-based equivalence.

CEO Device Classification - Class 1, General Controls

Product Code CEO Phosphomolybdate (colorimetric), Inorganic Phosphorus
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 862.1580
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 - CEO Phosphomolybdate (colorimetric), Inorganic Phosphorus

All 97
Devices cleared under the same product code (CEO) and FDA review panel - the closest regulatory comparables to K792401.
KING DIAGNOSTICS PHOSPHORUS TEST
K811749 · King Diagnostics, Inc. · Jul 1981
REAGENT FOR DETERM. INORGANIC/PHOSPHORUS
K800690 · Diagnostic Solutions, Inc. · May 1980
SANDARE FAST 340 PHOSPHOROUS PROCEDURE
K800297 · Sandare Chemical Co., Inc. · Mar 1980
INORGANIC PHOSPHORUS REAGENT
K791708 · Gilford Diagnostics · Sep 1979
SERUM, INORGANIC PHOSPHOROUS
K790021 · Fisher Scientific Co., LLC · Feb 1979
REAGENT SYSTEM, INORGANIC PHOSPHORUS
K781806 · Sigma Chemical Co. · Jan 1979