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URISCAN S-300 SEMI-AUTOMATED URINE CHEMISTRY ANALYZER

K980047 Class I Traditional
Decision Date
1998-06-10
Sponsor / Applicant
Yeongdong Pharmaceutical Corp.

Technical Specification

510(k) Submission ID K980047
Product Code KQO
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2900
Decision Date 1998-06-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

URISCAN S-300 SEMI-AUTOMATED URINE CHEMISTRY ANALYZER received FDA 510(k) clearance under submission number K980047, sponsored by Yeongdong Pharmaceutical Corp.. 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 1998-06-10.

Classification & Regulation

This clearance is catalogued under FDA product code KQO and 21 CFR 862.2900, within the Clinical Chemistry review panel as a Class I device.