meddevicedb.com FDA Device Reference

SOMATOM PLUS 4WITH VOLUME ZOOM CT SCANNERS

K982349 Class II Traditional
Decision Date
1998-09-30
Sponsor / Applicant
Siemens Medical Solutions USA, Inc.

Technical Specification

510(k) Submission ID K982349
Product Code JAK
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1750
Decision Date 1998-09-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SOMATOM PLUS 4WITH VOLUME ZOOM CT SCANNERS received FDA 510(k) clearance under submission number K982349, sponsored by Siemens Medical Solutions USA, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1998-09-30.

Classification & Regulation

This clearance is catalogued under FDA product code JAK and 21 CFR 892.1750, within the Radiology review panel as a Class II device.