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CENTRICITY PACS WEB DIAGNOSTIC

K083018 Class II Special
Decision Date
2008-11-14
Sponsor / Applicant
Ge Healthcare Dynamic Imaging Solutions

Technical Specification

510(k) Submission ID K083018
Product Code LLZ
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2050
Decision Date 2008-11-14
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CENTRICITY PACS WEB DIAGNOSTIC received FDA 510(k) clearance under submission number K083018, sponsored by Ge Healthcare Dynamic Imaging Solutions. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2008-11-14.

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.