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BALLOON TEMP. PACING CATHETER

K822003 Class II Traditional
Decision Date
1982-10-15
Sponsor / Applicant
Ziehm International, Inc.

Technical Specification

510(k) Submission ID K822003
Product Code LDF
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.3680
Decision Date 1982-10-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BALLOON TEMP. PACING CATHETER received FDA 510(k) clearance under submission number K822003, sponsored by Ziehm International, 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 1982-10-15.

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.