meddevicedb.com FDA Device Reference

OPEN END SPRING GUIDE

K832607 Class II Traditional
Decision Date
1983-12-27
Sponsor / Applicant
C.R. Bard, Inc.

Technical Specification

510(k) Submission ID K832607
Product Code DQX
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1330
Decision Date 1983-12-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OPEN END SPRING GUIDE received FDA 510(k) clearance under submission number K832607, 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 1983-12-27.

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.