Trans-Aire Rigid Gas Permeable Contact Lens

FDA 510(k) K952165 · Rand Scientific Corp.

Substantially Equivalent

510(k) numberK952165

Submission

Device name
Trans-Aire Rigid Gas Permeable Contact Lens
Applicant
Rand Scientific Corp.
Sacramento, CA, US
Received
April 3, 1995
Decision date
June 30, 1995
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
HQD – Lens, Contact (Other Material) - Daily
Device class
Class II (moderate risk)
Regulation
21 CFR 886.5916
Specialty
Ophthalmic

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K242393Acuity 181™ (tisilfocon A) and Acuity 181™ (tisilfocon A) with Tangible™ Hydra-PEG®…HQD · Traditional Acuity Polymers, Inc.11/01/2024SE
K241398SDJMASTERVISION (fluoroxyfocon A) Rigid Gas Permeable Contact LensesHQD · Traditional Tianjin Mastervision Technology Co., Ltd.10/22/2024SE
K241571BostonSight® Specialty LensesHQD · Traditional Boston Foundation For Sight, Inc. D/B/A…08/14/2024SE
K240618Acuity 200™ (fluoroxyfocon A) Rigid Gas Permeable Contact Lens; Acuity 100™ (hexafocon…HQD · Special Acuity Polymers, Inc.04/03/2024SE
K233325Visionary Optics Scleral Contact Lens (roflufocon D, roflufocon E, hexafocon A…HQD · Traditional Visionary Optics, LLC02/21/2024SE
K230965Acuity 100™ (hexafocon A) with Tangible™ Hydra-PEG®, TYRO™-97 (hofocon A) with Tangible™…HQD · Traditional Acuity Polymers, Inc.06/16/2023SE
K230910NewVision SC (tisilfocon A) Scleral Lens; NewVision SC Daily Wear Ortho-K (tisilfocon A)…HQD · Traditional Acculens, Inc.06/16/2023SE
K221768Oxfore®100 (hexafocon A) Rigid Gas Permeable Contact LensesHQD · Traditional Paragon Vision Sciences, Inc.05/05/2023SE
K223394Visionary Optics Scleral Contact Lens (roflufocon D, roflufocon E, hexafocon A…HQD · Special Visionary Optics, LLC12/07/2022SE

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Questions and answers

When was Trans-Aire Rigid Gas Permeable Contact Lens cleared by the FDA?

Trans-Aire Rigid Gas Permeable Contact Lens (K952165) received a 510(k) decision of Substantially Equivalent on June 30, 1995, 88 days after the submission was received.

What is the product code of K952165?

The FDA product code is HQD – Lens, Contact (Other Material) - Daily, a Class II (moderate risk) device regulated under 21 CFR 886.5916.