meddevicedb.com FDA Device Reference

MULTICARE PLATINUM SYSTEM AND ACCESSORIES

K030666 Class II Special
Decision Date
2003-03-25
Sponsor / Applicant
Lorad, A Hologic Co.

Technical Specification

510(k) Submission ID K030666
Product Code IZH
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1710
Decision Date 2003-03-25
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MULTICARE PLATINUM SYSTEM AND ACCESSORIES received FDA 510(k) clearance under submission number K030666, sponsored by Lorad, A Hologic Co.. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2003-03-25.

Classification & Regulation

This clearance is catalogued under FDA product code IZH and 21 CFR 892.1710, within the Radiology review panel as a Class II device.