meddevicedb.com FDA Device Reference

SCAR HEAL

K971468 Class I Traditional
Decision Date
1997-06-10
Sponsor / Applicant
Specialty Systems, Inc.

Technical Specification

510(k) Submission ID K971468
Product Code MDA
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4025
Decision Date 1997-06-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SCAR HEAL received FDA 510(k) clearance under submission number K971468, sponsored by Specialty Systems, Inc.. 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 1997-06-10.

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.