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QUANTITATE URIC ACID VERIFIER SET

K944453 Class I Traditional
Decision Date
1994-11-22
Sponsor / Applicant
Beckman Instruments, Inc.

Technical Specification

510(k) Submission ID K944453
Product Code JJX
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1660
Decision Date 1994-11-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

QUANTITATE URIC ACID VERIFIER SET received FDA 510(k) clearance under submission number K944453, 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 1994-11-22.

Classification & Regulation

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