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ADC QS/IPD WORKSTATION

K010571 Class II Special
Decision Date
2001-03-28
Sponsor / Applicant
Agfa Corp.

Technical Specification

510(k) Submission ID K010571
Product Code LLZ
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2050
Decision Date 2001-03-28
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ADC QS/IPD WORKSTATION received FDA 510(k) clearance under submission number K010571, sponsored by Agfa Corp.. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2001-03-28.

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.