meddevicedb.com FDA Device Reference

THE SILENCER

K954530 Class II Traditional
Decision Date
1995-10-30
Sponsor / Applicant
Silent Knights Ventures, Inc.

Technical Specification

510(k) Submission ID K954530
Product Code LRK
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.5570
Decision Date 1995-10-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

THE SILENCER received FDA 510(k) clearance under submission number K954530, sponsored by Silent Knights Ventures, 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 LRK and 21 CFR 872.5570, within the Dental review panel as a Class II device.