meddevicedb.com FDA Device Reference

OLEEVA FOAM

K002109 Class I Traditional
Decision Date
2000-08-31
Sponsor / Applicant
Bio Med Sciences, Inc.

Technical Specification

510(k) Submission ID K002109
Product Code MDA
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4025
Decision Date 2000-08-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OLEEVA FOAM received FDA 510(k) clearance under submission number K002109, sponsored by Bio Med Sciences, 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 2000-08-31.

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.