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MODIFICATION TO: SECTRA IDS5 WORKSTATION

K051315 Class II Special
Decision Date
2005-06-15
Sponsor / Applicant
Sectra Imtec AB

Technical Specification

510(k) Submission ID K051315
Product Code LLZ
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2050
Decision Date 2005-06-15
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODIFICATION TO: SECTRA IDS5 WORKSTATION received FDA 510(k) clearance under submission number K051315, sponsored by Sectra Imtec AB. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2005-06-15.

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.