Cleared Traditional

K903432 - IMX FREE T3 CALCULATION (FDA 510(k) Clearance)

Sep 1990
Decision
38d
Days
Class 2
Risk

K903432 is an FDA 510(k) clearance for the IMX FREE T3 CALCULATION. This device is classified as a Radioimmunoassay, Total Triiodothyronine (Class II - Special Controls, product code CDP).

Submitted by Abbott Laboratories (Abbott Park, US). The FDA issued a Cleared decision on September 7, 1990, 38 days after receiving the submission on July 31, 1990.

This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1710.

Submission Details

510(k) Number K903432 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 31, 1990
Decision Date September 07, 1990
Days to Decision 38 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary

Device Classification

Product Code CDP — Radioimmunoassay, Total Triiodothyronine
Device Class Class II - Special Controls
CFR Regulation 21 CFR 862.1710