meddevicedb.com FDA Device Reference

MASK SURGICAL

K963568 Class II Traditional
Decision Date
1997-02-25
Sponsor / Applicant
The Innovative Approach, Corp.

Technical Specification

510(k) Submission ID K963568
Product Code FXX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 1997-02-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MASK SURGICAL received FDA 510(k) clearance under submission number K963568, sponsored by The Innovative Approach, Corp.. 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 1997-02-25.

Classification & Regulation

This clearance is catalogued under FDA product code FXX and 21 CFR 878.4040, within the General, Plastic Surgery review panel as a Class II device.