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CALCIUM/LITHIUM TEST BECKMAN SYNCHRON EL-ISE ANALY

K914510 Class II Traditional
Decision Date
1991-11-19
Sponsor / Applicant
Beckman Instruments, Inc.

Technical Specification

510(k) Submission ID K914510
Product Code JFN
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1145
Decision Date 1991-11-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CALCIUM/LITHIUM TEST BECKMAN SYNCHRON EL-ISE ANALY received FDA 510(k) clearance under submission number K914510, 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 1991-11-19.

Classification & Regulation

This clearance is catalogued under FDA product code JFN and 21 CFR 862.1145, within the Clinical Chemistry review panel as a Class II device.