meddevicedb.com FDA Device Reference

EUPALAMUS DEFLECTABLE STYLET, MODEL 01545

K002534 Class II Traditional
Decision Date
2000-10-18
Sponsor / Applicant
Eupalamus, LLC

Technical Specification

510(k) Submission ID K002534
Product Code DRB
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1380
Decision Date 2000-10-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EUPALAMUS DEFLECTABLE STYLET, MODEL 01545 received FDA 510(k) clearance under submission number K002534, sponsored by Eupalamus, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2000-10-18.

Classification & Regulation

This clearance is catalogued under FDA product code DRB and 21 CFR 870.1380, within the Cardiovascular review panel as a Class II device.