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EVT EXPANDABLE SHEATH

K970470 Class II Traditional
Decision Date
1997-07-31
Sponsor / Applicant
Guidant Cardiac and Vascular Surgery

Technical Specification

510(k) Submission ID K970470
Product Code DRE
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1310
Decision Date 1997-07-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EVT EXPANDABLE SHEATH received FDA 510(k) clearance under submission number K970470, sponsored by Guidant Cardiac and Vascular Surgery. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1997-07-31.

Classification & Regulation

This clearance is catalogued under FDA product code DRE and 21 CFR 870.1310, within the Cardiovascular review panel as a Class II device.