meddevicedb.com FDA Device Reference

EMM EQUIPMENT COVER-POLYTHYLENE

K101689 Class II Traditional
Decision Date
2010-09-20
Sponsor / Applicant
Exact Medical Manufacturing, Inc.

Technical Specification

510(k) Submission ID K101689
Product Code KKX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4370
Decision Date 2010-09-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EMM EQUIPMENT COVER-POLYTHYLENE received FDA 510(k) clearance under submission number K101689, sponsored by Exact Medical Manufacturing, 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 2010-09-20.

Classification & Regulation

This clearance is catalogued under FDA product code KKX and 21 CFR 878.4370, within the General, Plastic Surgery review panel as a Class II device.