meddevicedb.com FDA Device Reference

HYDROL

K760660 Class II Traditional
Decision Date
1976-09-27
Sponsor / Applicant
Septodont, Inc.

Technical Specification

510(k) Submission ID K760660
Product Code LBH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3260
Decision Date 1976-09-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HYDROL received FDA 510(k) clearance under submission number K760660, sponsored by Septodont, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1976-09-27.

Classification & Regulation

This clearance is catalogued under FDA product code LBH and 21 CFR 872.3260, within the Dental review panel as a Class II device.