meddevicedb.com FDA Device Reference

OCUCARE ULTRASOUND TIP & FREEDOM PACK

K834543 Class II Traditional
Decision Date
1984-03-16
Sponsor / Applicant
Intermedics Intraocular, Inc.

Technical Specification

510(k) Submission ID K834543
Product Code HQC
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.4670
Decision Date 1984-03-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OCUCARE ULTRASOUND TIP & FREEDOM PACK received FDA 510(k) clearance under submission number K834543, sponsored by Intermedics Intraocular, 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 1984-03-16.

Classification & Regulation

This clearance is catalogued under FDA product code HQC and 21 CFR 886.4670, within the Ophthalmic review panel as a Class II device.