meddevicedb.com FDA Device Reference

OPHTHALMIC SURGICAL SPECULUM

K863664 Class I Traditional
Decision Date
1986-09-25
Sponsor / Applicant
Myocure, Inc.

Technical Specification

510(k) Submission ID K863664
Product Code HNC
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.4350
Decision Date 1986-09-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OPHTHALMIC SURGICAL SPECULUM received FDA 510(k) clearance under submission number K863664, sponsored by Myocure, 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 1986-09-25.

Classification & Regulation

This clearance is catalogued under FDA product code HNC and 21 CFR 886.4350, within the Ophthalmic review panel as a Class I device.