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OMNIPICC PI

K051102 Class II Traditional
Decision Date
2005-11-23
Sponsor / Applicant
Rita Medical Systems, Inc.

Technical Specification

510(k) Submission ID K051102
Product Code LJS
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5970
Decision Date 2005-11-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OMNIPICC PI received FDA 510(k) clearance under submission number K051102, sponsored by Rita Medical Systems, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2005-11-23.

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.