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INQUIRY OPTIMA PLUS STEERABLE ELECTROPHYSIOLOGY CATHETER

K060757 Class II Special
Decision Date
2006-04-19
Sponsor / Applicant
Irvine Biomedical, Inc.

Technical Specification

510(k) Submission ID K060757
Product Code DRF
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1220
Decision Date 2006-04-19
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

INQUIRY OPTIMA PLUS STEERABLE ELECTROPHYSIOLOGY CATHETER received FDA 510(k) clearance under submission number K060757, sponsored by Irvine Biomedical, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2006-04-19.

Classification & Regulation

This clearance is catalogued under FDA product code DRF and 21 CFR 870.1220, within the Cardiovascular review panel as a Class II device.