Cleared Traditional

K000600 - SYVA EMIT 2000 THYROXINE ASSAY, CALIBRATORS (FDA 510(k) Clearance)

Mar 2000
Decision
33d
Days
Class 2
Risk

K000600 is an FDA 510(k) clearance for the SYVA EMIT 2000 THYROXINE ASSAY, CALIBRATORS. This device is classified as a Enzyme Immunoassay, Non-radiolabeled, Total Thyroxine (Class II - Special Controls, product code KLI).

Submitted by Syva Co., Dade Behring, Inc. (San Jose, US). The FDA issued a Cleared decision on March 27, 2000, 33 days after receiving the submission on February 23, 2000.

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

Submission Details

510(k) Number K000600 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 23, 2000
Decision Date March 27, 2000
Days to Decision 33 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary Summary PDF

Device Classification

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