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DVT SCANNER

K051980 Class II Traditional
Decision Date
2005-08-19
Sponsor / Applicant
Imaging Sciences Intl., Inc.

Technical Specification

510(k) Submission ID K051980
Product Code JAK
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1750
Decision Date 2005-08-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DVT SCANNER received FDA 510(k) clearance under submission number K051980, sponsored by Imaging Sciences Intl., Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2005-08-19.

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.