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ILT CO2 SURGICAL LASER FOR ORAL SOFT TISSUE PROCED

K914726 Class II Traditional
Decision Date
1991-12-17
Sponsor / Applicant
Ion Laser Technology

Technical Specification

510(k) Submission ID K914726
Product Code GEX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4810
Decision Date 1991-12-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ILT CO2 SURGICAL LASER FOR ORAL SOFT TISSUE PROCED received FDA 510(k) clearance under submission number K914726, sponsored by Ion Laser Technology. 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 1991-12-17.

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.