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RIAUSE AUTO PROCESSOR

K801030 Class I Traditional
Decision Date
1980-05-28
Sponsor / Applicant
Electro-Nucleonics Laboratories, Inc.

Technical Specification

510(k) Submission ID K801030
Product Code JQW
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2750
Decision Date 1980-05-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RIAUSE AUTO PROCESSOR received FDA 510(k) clearance under submission number K801030, sponsored by Electro-Nucleonics Laboratories, 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 1980-05-28.

Classification & Regulation

This clearance is catalogued under FDA product code JQW and 21 CFR 862.2750, within the Clinical Chemistry review panel as a Class I device.