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KEATES IRRIGATION/ASPIRATION/VITREOUS CUTTER 5000

K853308 Class II Traditional
Decision Date
1985-10-04
Sponsor / Applicant
Frigitronics of Connecticut, Inc.

Technical Specification

510(k) Submission ID K853308
Product Code HQE
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.4150
Decision Date 1985-10-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

KEATES IRRIGATION/ASPIRATION/VITREOUS CUTTER 5000 received FDA 510(k) clearance under submission number K853308, sponsored by Frigitronics of Connecticut, 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 1985-10-04.

Classification & Regulation

This clearance is catalogued under FDA product code HQE and 21 CFR 886.4150, within the Ophthalmic review panel as a Class II device.