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POWERPICC

K053501 Class II Special
Decision Date
2006-01-13
Sponsor / Applicant
Bard Access Systems, Inc.

Technical Specification

510(k) Submission ID K053501
Product Code LJS
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5970
Decision Date 2006-01-13
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

POWERPICC received FDA 510(k) clearance under submission number K053501, sponsored by Bard Access Systems, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2006-01-13.

Classification & Regulation

This clearance is catalogued under FDA product code LJS and 21 CFR 880.5970, within the General Hospital review panel as a Class II device.