Cleared Traditional

K781996 - ACID REAGENT, URIC SINGLE VIAL

K781996 is an FDA 510(k) clearance for ACID REAGENT, manufactured by Calbiochem-Behring Corp.. The device is a Class 1 Chemistry device with product code CDO cleared through the Traditional 510(k) pathway after a 35-day FDA review.

K781996 · Calbiochem-Behring Corp. · Chemistry device
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Jan 1979
Decision
35d
Days
Class 1
Risk

K781996 is an FDA 510(k) clearance for the ACID REAGENT, URIC SINGLE VIAL. Classified as Acid, Uric, Uricase (u.v.) (product code CDO), Class I - General Controls.

Submitted by Calbiochem-Behring Corp. (Mchenry, US). The FDA issued a Cleared decision on January 3, 1979 after a review of 35 days - a notably fast clearance cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1775 - 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 Calbiochem-Behring Corp. devices

FDA 510(k) Submission Details - K781996

510(k) Number K781996 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 29, 1978
Decision Date January 03, 1979
Days to Decision 35 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
53d faster than avg
Panel avg: 88d · This submission: 35d
Pathway characteristics
Predicate-based equivalence.

CDO Device Classification - Class 1, General Controls

Product Code CDO Acid, Uric, Uricase (u.v.)
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 862.1775
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 - CDO Acid, Uric, Uricase (u.v.)

All 26
Devices cleared under the same product code (CDO) and FDA review panel - the closest regulatory comparables to K781996.
URIC ACID/ALDH
K802371 · Boehringer Mannheim Corp. · Oct 1980
CENTRIFICHEM URIC ACID
K800130 · Union Carbide Corp. · Feb 1980
UV URIC ACID DETERMINATION
K790834 · The Dow Chemical Co. · Jun 1979
PRINCETON BIOMEDIX URICASE (UV)
K780859 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Jul 1978
MULTISTAT III URIC ACID TEST
K771509 · Instrumentation Laboratory CO · Sep 1977
IN VITRO DIAG. FOR URIC ACID
K770767 · Smithkline Diagnostics, Inc. · Jul 1977