meddevicedb.com FDA Device Reference

MDT STERIGRIP DISPOSABLE, SOFT COVER, LIGHT HANDLE

K954940 Class II Traditional
Decision Date
1996-01-17
Sponsor / Applicant
Mdt Biologic Co.

Technical Specification

510(k) Submission ID K954940
Product Code FTA
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4580
Decision Date 1996-01-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MDT STERIGRIP DISPOSABLE, SOFT COVER, LIGHT HANDLE received FDA 510(k) clearance under submission number K954940, sponsored by Mdt Biologic Co.. 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 1996-01-17.

Classification & Regulation

This clearance is catalogued under FDA product code FTA and 21 CFR 878.4580, within the General, Plastic Surgery review panel as a Class II device.