meddevicedb.com FDA Device Reference

ROCS ULTRASEED

K984241 Class II Traditional
Decision Date
1999-05-12
Sponsor / Applicant
Radiation Oncology Computer Systems

Technical Specification

510(k) Submission ID K984241
Product Code IYE
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.5050
Decision Date 1999-05-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ROCS ULTRASEED received FDA 510(k) clearance under submission number K984241, sponsored by Radiation Oncology Computer Systems. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1999-05-12.

Classification & Regulation

This clearance is catalogued under FDA product code IYE and 21 CFR 892.5050, within the Radiology review panel as a Class II device.