Charter Hard Contact Lens Cleaning Solution

FDA 510(k) K865111 · Paco Pharmaceutical Services, Inc.

Substantially Equivalent

510(k) numberK865111

Submission

Device name
Charter Hard Contact Lens Cleaning Solution
Applicant
Paco Pharmaceutical Services, Inc.
Lakewood, NJ, US
Received
December 31, 1986
Decision date
January 20, 1987
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
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
K862811Aqualux Lens CaseHPX · Traditional Safeway Products, Inc.09/03/1986SE

More from Safeway Products, Inc.

510(k)DeviceDecision
K863974Charter Laboratories Inc. Lens LubricantHPX · Traditional 11/10/1986SE
K862952Charter Wetting Solution for Hard Contact LensesHPX · Traditional 09/25/1986SE
K843797Sterile Saline SolutionBSY · Traditional 01/18/1985SE
K843796Sterile Water · Traditional 12/10/1984SE
K761093BandageNAD · Traditional 01/06/1977SE

Questions and answers

When was Charter Hard Contact Lens Cleaning Solution cleared by the FDA?

Charter Hard Contact Lens Cleaning Solution (K865111) received a 510(k) decision of Substantially Equivalent on January 20, 1987, 20 days after the submission was received.

What is the product code of K865111?

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