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USCI TEMP. ATRIO-VENTRICULAR ELECTRODE

K830094 Class II Traditional
Decision Date
1983-02-18
Sponsor / Applicant
C.R. Bard, Inc.

Technical Specification

510(k) Submission ID K830094
Product Code LDF
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.3680
Decision Date 1983-02-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

USCI TEMP. ATRIO-VENTRICULAR ELECTRODE received FDA 510(k) clearance under submission number K830094, sponsored by C.R. Bard, 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 1983-02-18.

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.