Ocular Infusion Cannula System

FDA 510(k) K901618 · Tamcenan Corp.

Substantially Equivalent

510(k) numberK901618

Submission

Device name
Ocular Infusion Cannula System
Applicant
Tamcenan Corp.
Sioux Falls, SD, US
Received
April 6, 1990
Decision date
May 31, 1990
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
HMX – Cannula, Ophthalmic
Device class
Class I (low risk)
Regulation
21 CFR 886.4350
Specialty
Ophthalmic

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K970873Endosoft Soft Tip Needle (20 Ga. and 19 Ga.)HMX · Traditional American Medical Devices, Inc.05/20/1997SE
K943932Steriseal Ophthalmic CannulaHMX · Traditional Pharma-Plast, Ltd.01/18/1995SE
K942403Infusion CannulaHMX · Traditional Microsurgical Technology, Inc.08/17/1994SE
K934844Inter Tip THMX · Traditional Microsurgical Technology, Inc.04/19/1994SE
K930113Kirwan Irrigation/Aspiration HandpieceHMX · Traditional Kirwan Surgical Products, Inc.02/17/1994SE
K921488Aspirating Endo Ocular Probe W/IlluminationHMX · Traditional Surgical Technologies, Inc.05/07/1992SE
K915074Irrigator/Aspirator ProbeHMX · Traditional Biomedical Dynamics, Inc.02/05/1992SE
K904074Vitreoretinal Infusion CannulaHMX · Traditional Visitec Co.02/26/1991SE

More from Visitec Co.

510(k)DeviceDecision
K905750Lacrimal PlugLZU · Traditional 03/14/1991SE
K902308Tamcenan Ocular Explants and BandsHQX · Traditional 06/19/1990SE

Questions and answers

When was Ocular Infusion Cannula System cleared by the FDA?

Ocular Infusion Cannula System (K901618) received a 510(k) decision of Substantially Equivalent on May 31, 1990, 55 days after the submission was received.

What is the product code of K901618?

The FDA product code is HMX – Cannula, Ophthalmic, a Class I (low risk) device regulated under 21 CFR 886.4350.