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AUTOMATED BIOCHEMICAL ANALYZER (WAK0-20R & 30R)

K912024 Class I Traditional
Decision Date
1991-07-19
Sponsor / Applicant
Wako Chemicals USA, Inc.

Technical Specification

510(k) Submission ID K912024
Product Code JJE
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2160
Decision Date 1991-07-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AUTOMATED BIOCHEMICAL ANALYZER (WAK0-20R & 30R) received FDA 510(k) clearance under submission number K912024, sponsored by Wako Chemicals USA, 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 1991-07-19.

Classification & Regulation

This clearance is catalogued under FDA product code JJE and 21 CFR 862.2160, within the Clinical Chemistry review panel as a Class I device.