Cleared Traditional

K770070 - ENIT ABA THYROXINE ASSAY (FDA 510(k) Clearance)

Jan 1977
Decision
8d
Days
Class 2
Risk

K770070 is an FDA 510(k) clearance for the ENIT ABA THYROXINE ASSAY. This device is classified as a Enzyme Immunoassay, Non-radiolabeled, Total Thyroxine (Class II - Special Controls, product code KLI).

Submitted by Syva Co. (Walker, US). The FDA issued a Cleared decision on January 21, 1977, 8 days after receiving the submission on January 13, 1977.

This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1700.

Submission Details

510(k) Number K770070 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 13, 1977
Decision Date January 21, 1977
Days to Decision 8 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary

Device Classification

Product Code KLI — Enzyme Immunoassay, Non-radiolabeled, Total Thyroxine
Device Class Class II - Special Controls
CFR Regulation 21 CFR 862.1700