meddevicedb.com FDA Device Reference

MENTOR WET-FIELD*II COAGULATOR

K881001 Class II Traditional
Decision Date
1988-05-13
Sponsor / Applicant
Mentor O & O, Inc.

Technical Specification

510(k) Submission ID K881001
Product Code HQQ
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.4100
Decision Date 1988-05-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MENTOR WET-FIELD*II COAGULATOR received FDA 510(k) clearance under submission number K881001, sponsored by Mentor O & O, 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 1988-05-13.

Classification & Regulation

This clearance is catalogued under FDA product code HQQ and 21 CFR 886.4100, within the Ophthalmic review panel as a Class II device.