meddevicedb.com FDA Device Reference

ACTIVHEAL SCAR MANAGEMENT DRESSING

K010245 Class I Traditional
Decision Date
2001-04-25
Sponsor / Applicant
Advanced Medical Solutions, Ltd.

Technical Specification

510(k) Submission ID K010245
Product Code MDA
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4025
Decision Date 2001-04-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ACTIVHEAL SCAR MANAGEMENT DRESSING received FDA 510(k) clearance under submission number K010245, sponsored by Advanced Medical Solutions, Ltd.. 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 2001-04-25.

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.