meddevicedb.com FDA Device Reference

CONNECT

K954689 Class II Traditional
Decision Date
1995-10-30
Sponsor / Applicant
Sybron Dental Specialties, Inc.

Technical Specification

510(k) Submission ID K954689
Product Code EBI
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3760
Decision Date 1995-10-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CONNECT received FDA 510(k) clearance under submission number K954689, sponsored by Sybron Dental Specialties, 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 1995-10-30.

Classification & Regulation

This clearance is catalogued under FDA product code EBI and 21 CFR 872.3760, within the Dental review panel as a Class II device.