meddevicedb.com FDA Device Reference

PA GEL 35% IN BLUE AND PA GEL 10% IN GREEN OR BLUE

K993716 Class II Traditional
Decision Date
1999-12-21
Sponsor / Applicant
Harry J. Bosworth Co.

Technical Specification

510(k) Submission ID K993716
Product Code EBF
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3690
Decision Date 1999-12-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PA GEL 35% IN BLUE AND PA GEL 10% IN GREEN OR BLUE received FDA 510(k) clearance under submission number K993716, sponsored by Harry J. Bosworth Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1999-12-21.

Classification & Regulation

This clearance is catalogued under FDA product code EBF and 21 CFR 872.3690, within the Dental review panel as a Class II device.