meddevicedb.com FDA Device Reference

BIOPSY PUNCH, SURGICAL

K933670 Class I Traditional
Decision Date
1994-01-07
Sponsor / Applicant
Byron Medical

Technical Specification

510(k) Submission ID K933670
Product Code EME
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4565
Decision Date 1994-01-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BIOPSY PUNCH, SURGICAL received FDA 510(k) clearance under submission number K933670, sponsored by Byron Medical. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1994-01-07.

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.