Cleared Traditional

K863531 - IQ IMMUNOCHEMISTRY SYSTEM (FDA 510(k) Clearance)

Oct 1986
Decision
40d
Days
Class 1
Risk

K863531 is an FDA 510(k) clearance for the IQ IMMUNOCHEMISTRY SYSTEM. This device is classified as a Analyzer, Chemistry (photometric, Discrete), For Clinical Use (Class I - General Controls, product code JJE).

Submitted by Bd Becton Dickinson Vacutainer Systems Preanalytic (Franklin Lakes, US). The FDA issued a Cleared decision on October 20, 1986, 40 days after receiving the submission on September 10, 1986.

This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.2160.

Submission Details

510(k) Number K863531 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 10, 1986
Decision Date October 20, 1986
Days to Decision 40 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary

Device Classification

Product Code JJE — Analyzer, Chemistry (photometric, Discrete), For Clinical Use
Device Class Class I - General Controls
CFR Regulation 21 CFR 862.2160