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ULTRASONIC TIPS

K812126 Class II Traditional
Decision Date
1981-09-18
Sponsor / Applicant
CooperVision, Inc.

Technical Specification

510(k) Submission ID K812126
Product Code HQC
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.4670
Decision Date 1981-09-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ULTRASONIC TIPS received FDA 510(k) clearance under submission number K812126, sponsored by CooperVision, 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 1981-09-18.

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.