meddevicedb.com FDA Device Reference

ADC PEDIATRIC

K012750 Class II Traditional
Decision Date
2001-11-14
Sponsor / Applicant
Agfa Corp.

Technical Specification

510(k) Submission ID K012750
Product Code MQB
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1680
Decision Date 2001-11-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ADC PEDIATRIC received FDA 510(k) clearance under submission number K012750, sponsored by Agfa Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2001-11-14.

Classification & Regulation

This clearance is catalogued under FDA product code MQB and 21 CFR 892.1680, within the Radiology review panel as a Class II device.