Cleared Traditional

MAGNESIOMETER

K863069 · J. D. Assoc. · Chemistry
Dec 1986
Decision
141d
Days
Class 1
Risk

About This 510(k) Submission

K863069 is an FDA 510(k) clearance for the MAGNESIOMETER, a Photometric Method, Magnesium (Class I — General Controls, product code JGJ), submitted by J. D. Assoc. (Montclair, US). The FDA issued a Cleared decision on December 31, 1986, 141 days after receiving the submission on August 12, 1986. This device falls under the Chemistry review panel. Regulated under 21 CFR 862.1495.

Submission Details

510(k) Number K863069 FDA.gov
FDA Decision Cleared SESE
Date Received August 12, 1986
Decision Date December 31, 1986
Days to Decision 141 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary —

Device Classification

Product Code JGJ — Photometric Method, Magnesium
Device Class Class I — General Controls
CFR Regulation 21 CFR 862.1495

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