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DOCUMENT(TM) URIC ACID LINEARITY TEST SET

K893139 Class II Traditional
Decision Date
1989-07-20
Sponsor / Applicant
Casco Standards

Technical Specification

510(k) Submission ID K893139
Product Code JIT
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1150
Decision Date 1989-07-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DOCUMENT(TM) URIC ACID LINEARITY TEST SET received FDA 510(k) clearance under submission number K893139, sponsored by Casco Standards. 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 1989-07-20.

Classification & Regulation

This clearance is catalogued under FDA product code JIT and 21 CFR 862.1150, within the Clinical Chemistry review panel as a Class II device.