meddevicedb.com FDA Device Reference

MEPIFORM ADHERENT SILICONE DRESSING FOR SCAR CARE

K974354 Class I Traditional
Decision Date
1998-03-05
Sponsor / Applicant
Sca Molnlycke

Technical Specification

510(k) Submission ID K974354
Product Code MDA
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4025
Decision Date 1998-03-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MEPIFORM ADHERENT SILICONE DRESSING FOR SCAR CARE received FDA 510(k) clearance under submission number K974354, sponsored by Sca Molnlycke. 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 1998-03-05.

Classification & Regulation

This clearance is catalogued under FDA product code MDA and 21 CFR 878.4025, within the General, Plastic Surgery review panel as a Class I device.