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PLAQUEVIEW SOFTWARE, MODEL CSPV-0001A

K043111 Class II Traditional
Decision Date
2004-11-18
Sponsor / Applicant
Toshiba America Medical Systems, In.C

Technical Specification

510(k) Submission ID K043111
Product Code JAK
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1750
Decision Date 2004-11-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PLAQUEVIEW SOFTWARE, MODEL CSPV-0001A received FDA 510(k) clearance under submission number K043111, sponsored by Toshiba America Medical Systems, In.C. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2004-11-18.

Classification & Regulation

This clearance is catalogued under FDA product code JAK and 21 CFR 892.1750, within the Radiology review panel as a Class II device.