Cleared Traditional

K844990 - SYVA ADVANCE EMIT PHENYTOIN ASSAY (FDA 510(k) Clearance)

Jan 1985
Decision
28d
Days
Class 2
Risk

K844990 is an FDA 510(k) clearance for the SYVA ADVANCE EMIT PHENYTOIN ASSAY. This device is classified as a Fluorescent Immunoassay, Diphenylhydantoin (Class II - Special Controls, product code LES).

Submitted by Syva Co. (Palo Alto, US). The FDA issued a Cleared decision on January 23, 1985, 28 days after receiving the submission on December 26, 1984.

This device falls under the Toxicology FDA review panel. Regulated under 21 CFR 862.3350.

Submission Details

510(k) Number K844990 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 26, 1984
Decision Date January 23, 1985
Days to Decision 28 days
Submission Type Traditional
Review Panel Toxicology (TX)
Summary

Device Classification

Product Code LES — Fluorescent Immunoassay, Diphenylhydantoin
Device Class Class II - Special Controls
CFR Regulation 21 CFR 862.3350