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BIOMEK 1000C AUTOMATED LABORATORY WORK STATION

K871838 Class I Traditional
Decision Date
1987-05-26
Sponsor / Applicant
Beckman Instruments, Inc.

Technical Specification

510(k) Submission ID K871838
Product Code JJG
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2140
Decision Date 1987-05-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BIOMEK 1000C AUTOMATED LABORATORY WORK STATION received FDA 510(k) clearance under submission number K871838, 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 1987-05-26.

Classification & Regulation

This clearance is catalogued under FDA product code JJG and 21 CFR 862.2140, within the Clinical Chemistry review panel as a Class I device.