Contact Lens Cleaner

FDA 510(k) K812172 · Alcon Laboratories

Substantially Equivalent

510(k) numberK812172

Submission

Device name
Contact Lens Cleaner
Applicant
Alcon Laboratories
Mchenry, IL, US
Received
July 30, 1981
Decision date
August 31, 1981
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
HPX – Lens, Contact (Polymethylmethacrylate)
Device class
Unclassified

Other 510(k)s with product code HPX

510(k)DeviceApplicantDecision
K955777Pmma ClasicHPX · Traditional Rand Scientific Corp.05/16/1996SE
K940106Keratoplasty Suturing LensHPX · Traditional Visionary Technologies of Miami, Inc.05/25/1994SE
K913081Multi-View BifocalsHPX · Traditional Camp Contact Lenses10/23/1991SE
K897021Martin-Hensley Segment LensHPX · Traditional Bruce W. Martin O.D. and Edward Hensley06/22/1990SE
K895411Optikem Pmma Contact LensHPX · Traditional Optikem Polymers, Inc.02/27/1990SE
K874591Illuminating Infusion Contact Lens for Eye SurgeryHPX · Traditional Vitreo Dynamics, Co.05/03/1988SE
K865111Charter Hard Contact Lens Cleaning SolutionHPX · Traditional Paco Pharmaceutical Services, Inc.01/20/1987SE
K864343BL1 (Hard Contact Lens)HPX · Traditional Beta Labs, Inc.11/28/1986SE
K863974Charter Laboratories Inc. Lens LubricantHPX · Traditional Paco Pharmaceutical Services, Inc.11/10/1986SE
K862952Charter Wetting Solution for Hard Contact LensesHPX · Traditional Paco Pharmaceutical Services, Inc.09/25/1986SE

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Questions and answers

When was Contact Lens Cleaner cleared by the FDA?

Contact Lens Cleaner (K812172) received a 510(k) decision of Substantially Equivalent on August 31, 1981, 32 days after the submission was received.

What is the product code of K812172?

The FDA product code is HPX – Lens, Contact (Polymethylmethacrylate), a Unclassified device.