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LIQUID ASSAYED MULTIQUAL PREMIUM

K130162 Class I Traditional
Decision Date
2013-03-01
Sponsor / Applicant
Bio-Rad Laboratories

Technical Specification

510(k) Submission ID K130162
Product Code JJY
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1660
Decision Date 2013-03-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LIQUID ASSAYED MULTIQUAL PREMIUM received FDA 510(k) clearance under submission number K130162, sponsored by Bio-Rad Laboratories. 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 2013-03-01.

Classification & Regulation

This clearance is catalogued under FDA product code JJY and 21 CFR 862.1660, within the Clinical Chemistry review panel as a Class I device.