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S.L.T. CONTACT LASER SYSTEM

K855100 Class II Traditional
Decision Date
1986-02-26
Sponsor / Applicant
Surgical Laser Technologies, Inc.

Technical Specification

510(k) Submission ID K855100
Product Code LNK
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4810
Decision Date 1986-02-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

S.L.T. CONTACT LASER SYSTEM received FDA 510(k) clearance under submission number K855100, sponsored by Surgical Laser Technologies, 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 1986-02-26.

Classification & Regulation

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