meddevicedb.com FDA Device Reference

BOVO MOISTURE GUARD

K850988 Class I Traditional
Decision Date
1985-04-16
Sponsor / Applicant
E.H. Medical Co.

Technical Specification

510(k) Submission ID K850988
Product Code KHR
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6050
Decision Date 1985-04-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BOVO MOISTURE GUARD received FDA 510(k) clearance under submission number K850988, sponsored by E.H. Medical Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1985-04-16.

Classification & Regulation

This clearance is catalogued under FDA product code KHR and 21 CFR 872.6050, within the Dental review panel as a Class I device.