meddevicedb.com FDA Device Reference

SAFE MINI

K980974 Class II Traditional
Decision Date
2000-10-13
Sponsor / Applicant
Polystan A/S

Technical Specification

510(k) Submission ID K980974
Product Code DTZ
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4350
Decision Date 2000-10-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SAFE MINI received FDA 510(k) clearance under submission number K980974, sponsored by Polystan A/S. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2000-10-13.

Classification & Regulation

This clearance is catalogued under FDA product code DTZ and 21 CFR 870.4350, within the Cardiovascular review panel as a Class II device.