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FDI GLUCOSE CONTROL SOLUTIONS

K102260 Class I Traditional
Decision Date
2010-09-24
Sponsor / Applicant
Fujirebio Diagnostics,Inc.

Technical Specification

510(k) Submission ID K102260
Product Code JJX
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1660
Decision Date 2010-09-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FDI GLUCOSE CONTROL SOLUTIONS received FDA 510(k) clearance under submission number K102260, sponsored by Fujirebio Diagnostics,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 2010-09-24.

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.