BL1 (Hard Contact Lens)

FDA 510(k) K864343 · Beta Labs, Inc.

Substantially Equivalent

510(k) numberK864343

Submission

Device name
BL1 (Hard Contact Lens)
Applicant
Beta Labs, Inc.
Stoneham, MA, US
Received
November 4, 1986
Decision date
November 28, 1986
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
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

Questions and answers

When was BL1 (Hard Contact Lens) cleared by the FDA?

BL1 (Hard Contact Lens) (K864343) received a 510(k) decision of Substantially Equivalent on November 28, 1986, 24 days after the submission was received.

What is the product code of K864343?

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