meddevicedb.com FDA Device Reference

ACS.018 HI-TORQUE FLOPPY GUIDE WIRE - ACS HI-TORQUE FLOPPY EXTRA SUPPORT GUIDE WIRE

K934602 Class II Traditional
Decision Date
1993-12-16
Sponsor / Applicant
Advanced Cardiovascular Systems, Inc.

Technical Specification

510(k) Submission ID K934602
Product Code DQX
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1330
Decision Date 1993-12-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ACS.018 HI-TORQUE FLOPPY GUIDE WIRE - ACS HI-TORQUE FLOPPY EXTRA SUPPORT GUIDE WIRE received FDA 510(k) clearance under submission number K934602, sponsored by Advanced Cardiovascular Systems, 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 1993-12-16.

Classification & Regulation

This clearance is catalogued under FDA product code DQX and 21 CFR 870.1330, within the Cardiovascular review panel as a Class II device.