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DIAGNOSTIC ELECTROPHYSIOLOGY CATHETER SYSTEM

K953651 Class II Traditional
Decision Date
1995-11-30
Sponsor / Applicant
Arrow Intl., Inc.

Technical Specification

510(k) Submission ID K953651
Product Code DRF
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1220
Decision Date 1995-11-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DIAGNOSTIC ELECTROPHYSIOLOGY CATHETER SYSTEM received FDA 510(k) clearance under submission number K953651, sponsored by Arrow Intl., 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 1995-11-30.

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.