meddevicedb.com FDA Device Reference

FAST-CATH INTRA-CARDIAC INTRODUCER

K982187 Class II Traditional
Decision Date
1998-09-16
Sponsor / Applicant
Daig Corp.

Technical Specification

510(k) Submission ID K982187
Product Code DYB
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1340
Decision Date 1998-09-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FAST-CATH INTRA-CARDIAC INTRODUCER received FDA 510(k) clearance under submission number K982187, sponsored by Daig Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1998-09-16.

Classification & Regulation

This clearance is catalogued under FDA product code DYB and 21 CFR 870.1340, within the Cardiovascular review panel as a Class II device.