Cleared Traditional

PHOSPHORUS REAGENT SET

K823691 · Omega Medical Electronics · Chemistry
Jan 1983
Decision
30d
Days
Class 1
Risk

About This 510(k) Submission

K823691 is an FDA 510(k) clearance for the PHOSPHORUS REAGENT SET, a Phosphomolybdate (colorimetric), Inorganic Phosphorus (Class I — General Controls, product code CEO), submitted by Omega Medical Electronics (Mchenry, US). The FDA issued a Cleared decision on January 7, 1983, 30 days after receiving the submission on December 8, 1982. This device falls under the Chemistry review panel. Regulated under 21 CFR 862.1580.

Submission Details

510(k) Number K823691 FDA.gov
FDA Decision Cleared SESE
Date Received December 08, 1982
Decision Date January 07, 1983
Days to Decision 30 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary —

Device Classification

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

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