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URS LP DIGITAL, MILLENNIUM, RADPRO

K042876 Class II Special
Decision Date
2004-11-18
Sponsor / Applicant
Sedecal., Sa.

Technical Specification

510(k) Submission ID K042876
Product Code KPR
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1680
Decision Date 2004-11-18
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

URS LP DIGITAL, MILLENNIUM, RADPRO received FDA 510(k) clearance under submission number K042876, sponsored by Sedecal., Sa.. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2004-11-18.

Classification & Regulation

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