Cleared Traditional

K810261 - EUROCHIMA UREA NITROGEN

K810261 is an FDA 510(k) clearance for EUROCHIMA UREA NITROGEN, manufactured by Volu Sol Medical Industries. The device is a Class 2 Chemistry device with product code CDL cleared through the Traditional 510(k) pathway after a 11-day FDA review.

K810261 · Volu Sol Medical Industries · Chemistry device
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Feb 1981
Decision
11d
Days
Class 2
Risk

K810261 is an FDA 510(k) clearance for the EUROCHIMA UREA NITROGEN. Classified as Berthelot Indophenol, Urea Nitrogen (product code CDL), Class II - Special Controls.

Submitted by Volu Sol Medical Industries (Mchenry, US). The FDA issued a Cleared decision on February 10, 1981 after a review of 11 days - a notably fast clearance cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1770 - 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 - K810261

510(k) Number K810261 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 30, 1981
Decision Date February 10, 1981
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. No clinical trials required.

CDL Device Classification - Class 2, Special Controls

Product Code CDL Berthelot Indophenol, Urea Nitrogen
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.1770
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 - CDL Berthelot Indophenol, Urea Nitrogen

All 12
Devices cleared under the same product code (CDL) and FDA review panel - the closest regulatory comparables to K810261.
UREAFAST
K863076 · J. D. Assoc. · Sep 1986
BUN (ENZYMATIC BERTHELOT) REAGENT SET
K860154 · Sterling Diagnostics, Inc. · Feb 1986
COLORIMETRIC BUN
K831414 · Bio-Analytics Laboratories, Inc. · Jun 1983
DATA-ZYME UREA NITROGEN, COLORIMETRIC
K801727 · Data Medical Associates, Inc. · Sep 1980
BUN-COLOR 2, BLOOD UREA NITROGEN TEST
K800902 · Sclavo, Inc. · Jun 1980
ELVI BLOOD UREA NITROGEN
K792417 · Volu Sol Medical Industries · Dec 1979