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CLEAR-PB LEAD PLASTIC OVERHEAD BARRIER 56-628

K952233 Class I Traditional
Decision Date
1995-06-16
Sponsor / Applicant
Victoreen, Inc.

Technical Specification

510(k) Submission ID K952233
Product Code EAK
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.6500
Decision Date 1995-06-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CLEAR-PB LEAD PLASTIC OVERHEAD BARRIER 56-628 received FDA 510(k) clearance under submission number K952233, sponsored by Victoreen, 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 1995-06-16.

Classification & Regulation

This clearance is catalogued under FDA product code EAK and 21 CFR 892.6500, within the Radiology review panel as a Class I device.