meddevicedb.com FDA Device Reference

MODIFIED ULTRA-FRESH ODOR REDUCING COMPOUND

K883023 Class I Traditional
Decision Date
1988-09-29
Sponsor / Applicant
Mentor Corp.

Technical Specification

510(k) Submission ID K883023
Product Code GDS
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5900
Decision Date 1988-09-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODIFIED ULTRA-FRESH ODOR REDUCING COMPOUND received FDA 510(k) clearance under submission number K883023, sponsored by Mentor Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 1988-09-29.

Classification & Regulation

This clearance is catalogued under FDA product code GDS and 21 CFR 876.5900, within the Gastroenterology, Urology review panel as a Class I device.