meddevicedb.com FDA Device Reference

MULTI-SNARE SET

K011783 Class II Traditional
Decision Date
2002-01-24
Sponsor / Applicant
Pfm Produkte Fur Die Medizin AG

Technical Specification

510(k) Submission ID K011783
Product Code DXE
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.5150
Decision Date 2002-01-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MULTI-SNARE SET received FDA 510(k) clearance under submission number K011783, sponsored by Pfm Produkte Fur Die Medizin AG. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2002-01-24.

Classification & Regulation

This clearance is catalogued under FDA product code DXE and 21 CFR 870.5150, within the Cardiovascular review panel as a Class II device.