meddevicedb.com FDA Device Reference

DART ALPHA-AMYLASE REAGENT SYSTEM

K834053 Class II Traditional
Decision Date
1984-02-04
Sponsor / Applicant
Coulter Electronics, Inc.

Technical Specification

510(k) Submission ID K834053
Product Code CIJ
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1070
Decision Date 1984-02-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DART ALPHA-AMYLASE REAGENT SYSTEM received FDA 510(k) clearance under submission number K834053, sponsored by Coulter Electronics, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 1984-02-04.

Classification & Regulation

This clearance is catalogued under FDA product code CIJ and 21 CFR 862.1070, within the Clinical Chemistry review panel as a Class II device.