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NIKON URINE REFRACTOMER SG-1

K802959 Class I Traditional
Decision Date
1980-12-19
Sponsor / Applicant
Nippon Kogaku, Inc.

Technical Specification

510(k) Submission ID K802959
Product Code JRE
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2800
Decision Date 1980-12-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NIKON URINE REFRACTOMER SG-1 received FDA 510(k) clearance under submission number K802959, sponsored by Nippon Kogaku, 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 1980-12-19.

Classification & Regulation

This clearance is catalogued under FDA product code JRE and 21 CFR 862.2800, within the Clinical Chemistry review panel as a Class I device.