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FDA 510(k)

MiiS Horus Eye Anterior Camera

K-Number: K193188 · 2020-01-14

ApplicantMedimaging Integrated Solution, Inc (Miis)
Decision Date2020-01-14
Product CodeHJO
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MiiS Horus Eye Anterior Camera is the device name listed in this FDA 510(k) record. The listed applicant is Medimaging Integrated Solution, Inc (Miis). It received FDA 510(k) clearance on 2020-01-14 under 510(k) number K193188. The device is classified under product code HJO. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MiiS Horus Eye Anterior Camera?

MiiS Horus Eye Anterior Camera is a medical device that received FDA 510(k) clearance on 2020-01-14. The listed applicant is Medimaging Integrated Solution, Inc (Miis). The 510(k) number is K193188.

When did MiiS Horus Eye Anterior Camera receive FDA 510(k) clearance?

MiiS Horus Eye Anterior Camera received FDA 510(k) clearance on 2020-01-14, under 510(k) number K193188.

Who is the listed applicant for MiiS Horus Eye Anterior Camera?

The FDA 510(k) record lists Medimaging Integrated Solution, Inc (Miis) as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MiiS Horus Eye Anterior Camera?

The FDA product code for MiiS Horus Eye Anterior Camera is HJO.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07495345Feasibility Study of a Novel Automated Slit Lamp Camera (Lightfield Medical Ophthalmic Camera Model Vscan001)COMPLETED

Other records listing Medimaging Integrated Solution, Inc (Miis) as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K253217MiiS Horus Arthroscope (EJA 100); MiiS Horus Endoscope Display System -Tablet (EDS 500); MiiS Horus Endoscope Display System -Video Box (EVS 700)K234113MiiS Horus Bronchoscope; MiiS Horus Endoscope Display System -Tablet; MiiS Horus Endoscope Display System -Video BoxK223926VersaVue Single-Use Flexible Cystoscope, VersaVue Tablet, and VersaVue Video BoxK214050ENT Nasopharyngoscope and AccessoriesK181260MiiS Horus Scope DPT 100K170470Digital Eye Anterior Camera

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Related Devices (Code: HJO)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K253834VISUREF 600Carl Zeiss Vision GmbHK231760HP-OCT (HP-OCT)Cylite Pty. , Ltd.K222372Kowa SL-19Kowa Company , Ltd.K182306Sunkingdom Slit LampChongqing Sunkingdom Medical Instrument Co., Ltd.K173771IOLMaster 700Carl Zeiss Meditec, AGK171877SLM-1ER, SLM-2ER, SLM-3ERChongqing Kanghua Ruiming S&T Co., Ltd.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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