Kowa SL-19

FDA 510(k) K222372 · Kowa Company , Ltd.

Substantially Equivalent

510(k) numberK222372

Submission

Device name
Kowa SL-19
Applicant
Kowa Company , Ltd.
Chofu-Shi, JP
Received
August 5, 2022
Decision date
November 21, 2022
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
HJO – Biomicroscope, Slit-Lamp, Ac-Powered
Device class
Class II (moderate risk)
Regulation
21 CFR 886.1850
Specialty
Ophthalmic

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K193188MiiS Horus Eye Anterior CameraHJO · Traditional Medimaging Integrated Solution, Inc (Miis)01/14/2020SE
K182306Sunkingdom Slit LampHJO · Traditional Chongqing Sunkingdom Medical Instrument Co., Ltd.11/22/2018SE
K173771IOLMaster 700HJO · Traditional Carl Zeiss Meditec, AG08/24/2018SE
K171877SLM-1ER, SLM-2ER, SLM-3ERHJO · Traditional Chongqing Kanghua Ruiming S&T Co., Ltd.12/21/2017SE
K170470Digital Eye Anterior CameraHJO · Traditional Medimaging Integrated Solution, Inc (Miis)10/06/2017SE
K162778Portable Slit Lamp MicroscopeHJO · Traditional Suzhou Kangjie Medical, Inc.07/21/2017SE
K162684SL 220HJO · Traditional Carl Zeiss Meditec, AG05/31/2017SE
K163564Slit Lamp SL-2000HJO · Traditional Nidek Co., Ltd.05/19/2017SE

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Questions and answers

When was Kowa SL-19 cleared by the FDA?

Kowa SL-19 (K222372) received a 510(k) decision of Substantially Equivalent on November 21, 2022, 108 days after the submission was received.

What is the product code of K222372?

The FDA product code is HJO – Biomicroscope, Slit-Lamp, Ac-Powered, a Class II (moderate risk) device regulated under 21 CFR 886.1850.