meddevicedb.com FDA Device Reference

JOTA DIAMOND DENTAL BURS

K802987 Class I Traditional
Decision Date
1980-12-30
Sponsor / Applicant
Swiss American Metal Craft Corp.

Technical Specification

510(k) Submission ID K802987
Product Code DZP
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4535
Decision Date 1980-12-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

JOTA DIAMOND DENTAL BURS received FDA 510(k) clearance under submission number K802987, sponsored by Swiss American Metal Craft Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1980-12-30.

Classification & Regulation

This clearance is catalogued under FDA product code DZP and 21 CFR 872.4535, within the Dental review panel as a Class I device.