meddevicedb.com FDA Device Reference

SECTOR SCANNER, SDU-100, COMPUTERIZED

K791040 Class II Traditional
Decision Date
1979-10-04
Sponsor / Applicant
Shimadzu Corp.

Technical Specification

510(k) Submission ID K791040
Product Code IYO
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1560
Decision Date 1979-10-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SECTOR SCANNER, SDU-100, COMPUTERIZED received FDA 510(k) clearance under submission number K791040, sponsored by Shimadzu 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 1979-10-04.

Classification & Regulation

This clearance is catalogued under FDA product code IYO and 21 CFR 892.1560, within the Radiology review panel as a Class II device.