meddevicedb.com FDA Device Reference

ST AIA-PACK CYSTATIN C, MODEL 025217

K093960 Class II Traditional
Decision Date
2010-09-14
Sponsor / Applicant
Tosoh Bioscience, Inc.

Technical Specification

510(k) Submission ID K093960
Product Code NDY
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1225
Decision Date 2010-09-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ST AIA-PACK CYSTATIN C, MODEL 025217 received FDA 510(k) clearance under submission number K093960, sponsored by Tosoh Bioscience, 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 2010-09-14.

Classification & Regulation

This clearance is catalogued under FDA product code NDY and 21 CFR 862.1225, within the Clinical Chemistry review panel as a Class II device.