meddevicedb.com FDA Device Reference

TAKE 1 BITE

K001876 Class II Traditional
Decision Date
2000-07-21
Sponsor / Applicant
Sybron Dental Specialties, Inc.

Technical Specification

510(k) Submission ID K001876
Product Code ELW
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3660
Decision Date 2000-07-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TAKE 1 BITE received FDA 510(k) clearance under submission number K001876, 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 2000-07-21.

Classification & Regulation

This clearance is catalogued under FDA product code ELW and 21 CFR 872.3660, within the Dental review panel as a Class II device.