meddevicedb.com FDA Device Reference

OCULAR FORCE GAUGE

K132917 Class II Traditional
Decision Date
2013-12-20
Sponsor / Applicant
Ocular Therapeutix, Inc.

Technical Specification

510(k) Submission ID K132917
Product Code HKY
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.1930
Decision Date 2013-12-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OCULAR FORCE GAUGE received FDA 510(k) clearance under submission number K132917, sponsored by Ocular Therapeutix, 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 2013-12-20.

Classification & Regulation

This clearance is catalogued under FDA product code HKY and 21 CFR 886.1930, within the Ophthalmic review panel as a Class II device.