meddevicedb.com FDA Device Reference

FLASH BOND

K920781 Class II Traditional
Decision Date
1992-04-21
Sponsor / Applicant
Advanced Orthodontics Systems, Inc.

Technical Specification

510(k) Submission ID K920781
Product Code DYH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3750
Decision Date 1992-04-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FLASH BOND received FDA 510(k) clearance under submission number K920781, sponsored by Advanced Orthodontics Systems, 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 1992-04-21.

Classification & Regulation

This clearance is catalogued under FDA product code DYH and 21 CFR 872.3750, within the Dental review panel as a Class II device.