meddevicedb.com FDA Device Reference

O.R. TIP CLEANER

K903610 Class II Traditional
Decision Date
1990-10-19
Sponsor / Applicant
Inman Liebelt Corp.

Technical Specification

510(k) Submission ID K903610
Product Code GEI
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4400
Decision Date 1990-10-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

O.R. TIP CLEANER received FDA 510(k) clearance under submission number K903610, sponsored by Inman Liebelt 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 1990-10-19.

Classification & Regulation

This clearance is catalogued under FDA product code GEI and 21 CFR 878.4400, within the General, Plastic Surgery review panel as a Class II device.