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ZYNERGY FEATHERPACE TRANSVENOUS BIPOLAR CATHETER, MODEL 04-X-02-3-10-3

K002481 Class II Traditional
Decision Date
2000-12-07
Sponsor / Applicant
Zcv ,Inc.

Technical Specification

510(k) Submission ID K002481
Product Code LDF
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.3680
Decision Date 2000-12-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ZYNERGY FEATHERPACE TRANSVENOUS BIPOLAR CATHETER, MODEL 04-X-02-3-10-3 received FDA 510(k) clearance under submission number K002481, sponsored by Zcv ,Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2000-12-07.

Classification & Regulation

This clearance is catalogued under FDA product code LDF and 21 CFR 870.3680, within the Cardiovascular review panel as a Class II device.