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PACING SYSTEM ANALYZER

K803313 Class II Traditional
Decision Date
1981-02-23
Sponsor / Applicant
Medtronic Vascular

Technical Specification

510(k) Submission ID K803313
Product Code DTE
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.3600
Decision Date 1981-02-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PACING SYSTEM ANALYZER received FDA 510(k) clearance under submission number K803313, sponsored by Medtronic Vascular. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1981-02-23.

Classification & Regulation

This clearance is catalogued under FDA product code DTE and 21 CFR 870.3600, within the Cardiovascular review panel as a Class II device.