Kestrel Contact Lens Storage Case(Polysulfone)

FDA 510(k) K853727 · Ryder Intl. Corp.

Substantially Equivalent

510(k) numberK853727

Submission

Device name
Kestrel Contact Lens Storage Case(Polysulfone)
Applicant
Ryder Intl. Corp.
Arab, AL, US
Received
September 6, 1985
Decision date
February 7, 1986
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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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K173365Bausch + Lomb Boston Scleral Lens CaseLRX · Traditional Bausch & Lomb, Incorporated11/17/2017SE
K171539Contact Lens CaseLRX · Traditional E-Link Plastic & Metal Industrial Co.,Ltd07/14/2017SE
K171163Contact Lens Case Round GlassesLRX · Traditional Fiftytwoways, Ltd.06/27/2017SE
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More from Ningbo Yinzhou Zonghai Artware Co., Ltd.

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K920064Opti-Lens Contact Lens CaseLRX · Traditional 03/04/1992SE
K915082Opti-Lens(Tm) Contact Lens CaseLRX · Traditional 01/13/1992SE
K881981Assist(Tm) Aseptic Syringe Irrigation SystemKOD · Traditional 08/02/1988SE
K870278Contact Lens Case W/Postive Heat Indi. Mod. #695LPN · Traditional 02/20/1987SE
K853729Kestrel Contact Lens Storage Case(Polystyrene)HPX · Traditional 12/13/1985SE
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Questions and answers

When was Kestrel Contact Lens Storage Case(Polysulfone) cleared by the FDA?

Kestrel Contact Lens Storage Case(Polysulfone) (K853727) received a 510(k) decision of Substantially Equivalent on February 7, 1986, 154 days after the submission was received.

What is the product code of K853727?

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