meddevicedb.com FDA Device Reference

MINICAM

K001541 Class I Traditional
Decision Date
2000-07-21
Sponsor / Applicant
Video Dental Concepts, Inc.

Technical Specification

510(k) Submission ID K001541
Product Code EIA
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6640
Decision Date 2000-07-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MINICAM received FDA 510(k) clearance under submission number K001541, sponsored by Video Dental Concepts, 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 2000-07-21.

Classification & Regulation

This clearance is catalogued under FDA product code EIA and 21 CFR 872.6640, within the Dental review panel as a Class I device.