meddevicedb.com FDA Device Reference

EASY-ON

K932998 Class I Traditional
Decision Date
1993-08-18
Sponsor / Applicant
Devon Industries, Inc.

Technical Specification

510(k) Submission ID K932998
Product Code GES
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4800
Decision Date 1993-08-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EASY-ON received FDA 510(k) clearance under submission number K932998, sponsored by Devon Industries, 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 1993-08-18.

Classification & Regulation

This clearance is catalogued under FDA product code GES and 21 CFR 878.4800, within the General, Plastic Surgery review panel as a Class I device.