meddevicedb.com FDA Device Reference

3M MINI-DRIVER ELECTRIC SYSTEM

K955098 Class I Traditional
Decision Date
1996-01-22
Sponsor / Applicant
3M Company

Technical Specification

510(k) Submission ID K955098
Product Code HWE
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4820
Decision Date 1996-01-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

3M MINI-DRIVER ELECTRIC SYSTEM received FDA 510(k) clearance under submission number K955098, sponsored by 3M Company. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1996-01-22.

Classification & Regulation

This clearance is catalogued under FDA product code HWE and 21 CFR 878.4820, within the General, Plastic Surgery review panel as a Class I device.