meddevicedb.com FDA Device Reference

EURO-MED LIGHT TOUCH BIOPSY PUNCH

K884740 Class I Traditional
Decision Date
1989-03-06
Sponsor / Applicant
Buckman Co., Inc.

Technical Specification

510(k) Submission ID K884740
Product Code EME
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4565
Decision Date 1989-03-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EURO-MED LIGHT TOUCH BIOPSY PUNCH received FDA 510(k) clearance under submission number K884740, sponsored by Buckman Co., 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 1989-03-06.

Classification & Regulation

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