meddevicedb.com FDA Device Reference

ND:YAG LASER SPECTACLES, MST MODEL #YLS-5

K883839 Class I Traditional
Decision Date
1988-12-09
Sponsor / Applicant
Marlo Surgical Technology

Technical Specification

510(k) Submission ID K883839
Product Code KYP
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5740
Decision Date 1988-12-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ND:YAG LASER SPECTACLES, MST MODEL #YLS-5 received FDA 510(k) clearance under submission number K883839, sponsored by Marlo Surgical Technology. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1988-12-09.

Classification & Regulation

This clearance is catalogued under FDA product code KYP and 21 CFR 880.5740, within the General Hospital review panel as a Class I device.