meddevicedb.com FDA Device Reference

PC LASER WITH SMART PLUG (PC EDO & DENTAL 200)

K963124 Class II Traditional
Decision Date
1996-11-08
Sponsor / Applicant
Fisma, Inc.

Technical Specification

510(k) Submission ID K963124
Product Code GEX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4810
Decision Date 1996-11-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PC LASER WITH SMART PLUG (PC EDO & DENTAL 200) received FDA 510(k) clearance under submission number K963124, sponsored by Fisma, 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 1996-11-08.

Classification & Regulation

This clearance is catalogued under FDA product code GEX and 21 CFR 878.4810, within the General, Plastic Surgery review panel as a Class II device.