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SLT CONTACT LASER SYSTEM ENDOPHOTOCOAGULATION

K882441 Class II Traditional
Decision Date
1988-09-26
Sponsor / Applicant
Surgical Laser Technologies, Inc.

Technical Specification

510(k) Submission ID K882441
Product Code HQB
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.4690
Decision Date 1988-09-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SLT CONTACT LASER SYSTEM ENDOPHOTOCOAGULATION received FDA 510(k) clearance under submission number K882441, sponsored by Surgical Laser Technologies, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 1988-09-26.

Classification & Regulation

This clearance is catalogued under FDA product code HQB and 21 CFR 886.4690, within the Ophthalmic review panel as a Class II device.