Quadraspheric Fundus Lens

FDA 510(k) K943125 · Volk Optical, Inc.

Substantially Equivalent

510(k) numberK943125

Submission

Device name
Quadraspheric Fundus Lens
Applicant
Volk Optical, Inc.
Cleveland, OH, US
Received
June 29, 1994
Decision date
September 2, 1994
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
HJK – Lens, Contact, Polymethylmethacrylate, Diagnostic
Device class
Class II (moderate risk)
Regulation
21 CFR 886.1385
Specialty
Ophthalmic

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K201909RxSight Contact LensHJK · Traditional Rxsight, Inc.09/10/2020SE
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K151961Volk Disposable Iridotomy Lens, Volk Disposable Capsulotomy LensHJK · Special Volk Optical, Inc.08/18/2015SE
K142715Sensor Medical Family of Vitrectomy Lenses and ProductsHJK · Traditional Sensor Medical Technology, LLC12/16/2014SE
K051630Super View Disposable Biom Lens SetHJK · Traditional Insight Instruments, Inc.06/29/2005SE
K051103Haag-Streit Contact Glasses Stery Cup, AccessoryHJK · Traditional Haag-Streit USA, Inc.06/07/2005SE
K050623Volk Disposable Vitrectomy Lenses, Models Volk Flat SSV D, Volk Afx SSV D, Volk 45 Prism…HJK · Special Volk Optical, Inc.03/28/2005SE
K033950Dorc Vitrectomy Lenses, Model 1284 SeriesHJK · Traditional Dutch Ophthalmic Research Center (D.O.R.C.)02/20/2004SE
K030054Disposable Vitrectomy Sets, Disposable Virectomy LensesHJK · Traditional Fci Ophthalmics, Inc.02/26/2003SE
K023221Contact Laser & Diagnostic LensesHJK · Special Volk Optical, Inc.10/11/2002SE

More from Volk Optical, Inc.

510(k)DeviceDecision
K151961Volk Disposable Iridotomy Lens, Volk Disposable Capsulotomy LensHJK · Special 08/18/2015SE
K050623Volk Disposable Vitrectomy Lenses, Models Volk Flat SSV D, Volk Afx SSV D, Volk 45 Prism…HJK · Special 03/28/2005SE
K023221Contact Laser & Diagnostic LensesHJK · Special 10/11/2002SE

Questions and answers

When was Quadraspheric Fundus Lens cleared by the FDA?

Quadraspheric Fundus Lens (K943125) received a 510(k) decision of Substantially Equivalent on September 2, 1994, 65 days after the submission was received.

What is the product code of K943125?

The FDA product code is HJK – Lens, Contact, Polymethylmethacrylate, Diagnostic, a Class II (moderate risk) device regulated under 21 CFR 886.1385.