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Lung Analysis Software

K151283 Class II Traditional
Decision Date
2015-10-30
Sponsor / Applicant
Vital Images, Inc.

Technical Specification

510(k) Submission ID K151283
Product Code JAK
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1750
Decision Date 2015-10-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Lung Analysis Software received FDA 510(k) clearance under submission number K151283, sponsored by Vital Images, 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 2015-10-30.

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.