meddevicedb.com FDA Device Reference

SURGILASE YAG 100 FOR GYNECOLOGY USE

K881499 Class II Traditional
Decision Date
1988-04-29
Sponsor / Applicant
Surgilase, Inc.

Technical Specification

510(k) Submission ID K881499
Product Code LLO
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.4500
Decision Date 1988-04-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SURGILASE YAG 100 FOR GYNECOLOGY USE received FDA 510(k) clearance under submission number K881499, sponsored by Surgilase, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ear, Nose, Throat review panel. The statutory decision date of record is 1988-04-29.

Classification & Regulation

This clearance is catalogued under FDA product code LLO and 21 CFR 874.4500, within the Ear, Nose, Throat review panel as a Class II device.