Cleared Traditional

URIC ACID

K850933 · Dilab, Inc. · Chemistry
Jun 1985
Decision
110d
Days
Class 1
Risk

About This 510(k) Submission

K850933 is an FDA 510(k) clearance for the URIC ACID, a Acid, Uric, Phosphotungstate Reduction (Class I — General Controls, product code CDH), submitted by Dilab, Inc. (Miami, US). The FDA issued a Cleared decision on June 25, 1985, 110 days after receiving the submission on March 7, 1985. This device falls under the Chemistry review panel. Regulated under 21 CFR 862.1775.

Submission Details

510(k) Number K850933 FDA.gov
FDA Decision Cleared SESE
Date Received March 07, 1985
Decision Date June 25, 1985
Days to Decision 110 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary —

Device Classification

Product Code CDH — Acid, Uric, Phosphotungstate Reduction
Device Class Class I — General Controls
CFR Regulation 21 CFR 862.1775

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