Sauflon Flat Lens Case/Sauflon 2003 Barrel Lens Case

FDA 510(k) K033656 · Sauflon Pharmaceuticals, Ltd.

Substantially Equivalent

510(k) numberK033656

Submission

Device name
Sauflon Flat Lens Case/Sauflon 2003 Barrel Lens Case
Applicant
Sauflon Pharmaceuticals, Ltd.
Twickenham, Middlesex, GB
Received
November 21, 2003
Decision date
February 2, 2004
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
LRX – Case, Contact Lens
Device class
Class II (moderate risk)
Regulation
21 CFR 886.5928
Specialty
Ophthalmic

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More from Ningbo Yinzhou Zonghai Artware Co., Ltd.

510(k)DeviceDecision
K133740Sauflon Clariti with Tint, Sauflon Clariti Toric with Tint, Sauflon Clariti Multifocal…LPL · Traditional 03/05/2014SE
K130342Sauflon Clariti (Somofilcon a) Soft (Hydrophilic) Contact Lens with UV BlockerLPL · Traditional 08/05/2013SE
K130331Sauflon Clariti 1 Day (Somofilcon a) Soft (Hydrophilic) Daily Disposable Contact Lens…MVN · Traditional 07/26/2013SE
K130734Sauflon Multipurpose SolutionLPN · Traditional 05/15/2013SE
K052832Sauflon New Day (Methafilcon a) Soft (Hydrophilic) Daily Disposable Contact LensesMVN · Traditional 05/15/2006SE
K052809Sauflon Flat Coloured Lens CaseLRX · Traditional 11/02/2005SE
K030278Sauflon Multipurpose Solution - No RubLPN · Traditional 07/30/2003SE
K013649Sauflon 55 UV Soft (Hydrophilic) Contact LensLPL · Traditional 12/26/2001SE
K010559Sauflon Multi Lens Care SystemLPN · Traditional 12/20/2001SE
K011456Delta Plus Multiaction Solution for Rigid Gas Permeable Contact LensesMRC · Traditional 07/17/2001SE

Questions and answers

When was Sauflon Flat Lens Case/Sauflon 2003 Barrel Lens Case cleared by the FDA?

Sauflon Flat Lens Case/Sauflon 2003 Barrel Lens Case (K033656) received a 510(k) decision of Substantially Equivalent on February 2, 2004, 73 days after the submission was received.

What is the product code of K033656?

The FDA product code is LRX – Case, Contact Lens, a Class II (moderate risk) device regulated under 21 CFR 886.5928.