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SILANE PRIMER

K954708 Class II Traditional
Decision Date
1995-10-30
Sponsor / Applicant
Sybron Dental Specialties, Inc.

Technical Specification

510(k) Submission ID K954708
Product Code KLE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3200
Decision Date 1995-10-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SILANE PRIMER received FDA 510(k) clearance under submission number K954708, 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 KLE and 21 CFR 872.3200, within the Dental review panel as a Class II device.