meddevicedb.com FDA Device Reference

BECKMAN LIQUID-STAT AST-UV LIQUID

K821433 Class II Traditional
Decision Date
1982-06-02
Sponsor / Applicant
Beckman Instruments, Inc.

Technical Specification

510(k) Submission ID K821433
Product Code CIT
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1100
Decision Date 1982-06-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BECKMAN LIQUID-STAT AST-UV LIQUID received FDA 510(k) clearance under submission number K821433, sponsored by Beckman Instruments, 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 1982-06-02.

Classification & Regulation

This clearance is catalogued under FDA product code CIT and 21 CFR 862.1100, within the Clinical Chemistry review panel as a Class II device.