meddevicedb.com FDA Device Reference

BREVET FLOSS PICK (AUTOCLAVE STERILIZER)

K895958 Class I Traditional
Decision Date
1989-12-04
Sponsor / Applicant
Brevet, Inc.

Technical Specification

510(k) Submission ID K895958
Product Code EKJ
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4565
Decision Date 1989-12-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BREVET FLOSS PICK (AUTOCLAVE STERILIZER) received FDA 510(k) clearance under submission number K895958, sponsored by Brevet, 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 1989-12-04.

Classification & Regulation

This clearance is catalogued under FDA product code EKJ and 21 CFR 872.4565, within the Dental review panel as a Class I device.