Cleared Traditional

K963827 - AXSYM FREE TRIIODOTHYRONINE (FREE T3) (FDA 510(k) Clearance)

Oct 1996
Decision
36d
Days
Class 2
Risk

K963827 is an FDA 510(k) clearance for the AXSYM FREE TRIIODOTHYRONINE (FREE T3). 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 October 30, 1996, 36 days after receiving the submission on September 24, 1996.

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

Submission Details

510(k) Number K963827 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 24, 1996
Decision Date October 30, 1996
Days to Decision 36 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary Summary PDF

Device Classification

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