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SITE 810E PHOTOCOAGULATOR AND ACCESSORIES

K895663 Class II Traditional
Decision Date
1989-12-04
Sponsor / Applicant
Site Microsurgical Systems, Inc.

Technical Specification

510(k) Submission ID K895663
Product Code GEX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4810
Decision Date 1989-12-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SITE 810E PHOTOCOAGULATOR AND ACCESSORIES received FDA 510(k) clearance under submission number K895663, sponsored by Site Microsurgical Systems, 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 1989-12-04.

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.