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PATIENTGALLERY IMAGING SOFTWARE

K070954 Class II Traditional
Decision Date
2007-04-20
Sponsor / Applicant
Raster Builders, Inc.

Technical Specification

510(k) Submission ID K070954
Product Code LLZ
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2050
Decision Date 2007-04-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PATIENTGALLERY IMAGING SOFTWARE received FDA 510(k) clearance under submission number K070954, sponsored by Raster Builders, 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 2007-04-20.

Classification & Regulation

This clearance is catalogued under FDA product code LLZ and 21 CFR 892.2050, within the Radiology review panel as a Class II device.