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I-125 SEEDS, CODE: 6711

K914281 Class II Traditional
Decision Date
1991-11-22
Sponsor / Applicant
Medi-Physics Inc. Dba Nycomed Amersham Imaging

Technical Specification

510(k) Submission ID K914281
Product Code KXK
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.5730
Decision Date 1991-11-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

I-125 SEEDS, CODE: 6711 received FDA 510(k) clearance under submission number K914281, 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 1991-11-22.

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.