Cleared Traditional

K971363 - SYNCHRON CX SYSTEMS PHOSPHORUS REAGENT (FDA 510(k) Clearance)

Apr 1997
Decision
14d
Days
Class 1
Risk

K971363 is an FDA 510(k) clearance for the SYNCHRON CX SYSTEMS PHOSPHORUS REAGENT. This device is classified as a Phosphomolybdate (colorimetric), Inorganic Phosphorus (Class I - General Controls, product code CEO).

Submitted by Carolina Liquid Chemistries Corp. (Brea, US). The FDA issued a Cleared decision on April 21, 1997, 14 days after receiving the submission on April 7, 1997.

This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1580.

Submission Details

510(k) Number K971363 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 07, 1997
Decision Date April 21, 1997
Days to Decision 14 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary Statement

Device Classification

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