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BECKMAN ICS CALIBRATOR

K812649 Class II Traditional
Decision Date
1981-10-19
Sponsor / Applicant
Beckman Instruments, Inc.

Technical Specification

510(k) Submission ID K812649
Product Code JIX
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1150
Decision Date 1981-10-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BECKMAN ICS CALIBRATOR received FDA 510(k) clearance under submission number K812649, 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 1981-10-19.

Classification & Regulation

This clearance is catalogued under FDA product code JIX and 21 CFR 862.1150, within the Clinical Chemistry review panel as a Class II device.