Cleared Traditional

K890451 - EMIT(R) D.A.U AMPHETAMINE CLASS LOW CALIBRATOR (FDA 510(k) Clearance)

Feb 1989
Decision
11d
Days
Class 2
Risk

K890451 is an FDA 510(k) clearance for the EMIT(R) D.A.U AMPHETAMINE CLASS LOW CALIBRATOR. This device is classified as a Calibrators, Drug Specific (Class II - Special Controls, product code DLJ).

Submitted by Syva Co. (Palo Alto, US). The FDA issued a Cleared decision on February 10, 1989, 11 days after receiving the submission on January 30, 1989.

This device falls under the Toxicology FDA review panel. Regulated under 21 CFR 862.3200.

Submission Details

510(k) Number K890451 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 30, 1989
Decision Date February 10, 1989
Days to Decision 11 days
Submission Type Traditional
Review Panel Toxicology (TX)
Summary

Device Classification

Product Code DLJ — Calibrators, Drug Specific
Device Class Class II - Special Controls
CFR Regulation 21 CFR 862.3200