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I-125 SEEDS CODE: 6702

K915156 Class II Traditional
Decision Date
1992-01-06
Sponsor / Applicant
Medi-Physics Inc. Dba Nycomed Amersham Imaging

Technical Specification

510(k) Submission ID K915156
Product Code KXK
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.5730
Decision Date 1992-01-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

I-125 SEEDS CODE: 6702 received FDA 510(k) clearance under submission number K915156, sponsored by Medi-Physics Inc. Dba Nycomed Amersham Imaging. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1992-01-06.

Classification & Regulation

This clearance is catalogued under FDA product code KXK and 21 CFR 892.5730, within the Radiology review panel as a Class II device.