meddevicedb.com FDA Device Reference

VIDEO PRINTER SYSTEM

K873419 Class I Traditional
Decision Date
1987-11-02
Sponsor / Applicant
Technology For Imaging, Inc.

Technical Specification

510(k) Submission ID K873419
Product Code KQM
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4160
Decision Date 1987-11-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VIDEO PRINTER SYSTEM received FDA 510(k) clearance under submission number K873419, sponsored by Technology For Imaging, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1987-11-02.

Classification & Regulation

This clearance is catalogued under FDA product code KQM and 21 CFR 878.4160, within the General, Plastic Surgery review panel as a Class I device.