MiiS Horus Eye Anterior Camera
K-Number: K193188 · 2020-01-14
Decision Date2020-01-14
Product CodeHJO
Advisory CommitteeOP
DecisionSubstantially Equivalent
Device Summary
MiiS Horus Eye Anterior Camera is a medical device manufactured by Medimaging Integrated Solution, Inc (Miis). It received FDA 510(k) clearance on 2020-01-14 under approval 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. It is manufactured by Medimaging Integrated Solution, Inc (Miis). The 510(k) number is K193188.
When was MiiS Horus Eye Anterior Camera approved by the FDA?
MiiS Horus Eye Anterior Camera received FDA 510(k) clearance on 2020-01-14, under approval number K193188.
What company makes MiiS Horus Eye Anterior Camera?
MiiS Horus Eye Anterior Camera is manufactured by Medimaging Integrated Solution, Inc (Miis).
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
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K170470Digital Eye Anterior Camera
K181260MiiS Horus Scope DPT 100
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K223926VersaVue Single-Use Flexible Cystoscope, VersaVue Tablet, and VersaVue Video Box
K234113MiiS Horus Bronchoscope; MiiS Horus Endoscope Display System -Tablet; MiiS Horus Endoscope Display System -Video Box
K253217MiiS Horus Arthroscope (EJA 100); MiiS Horus Endoscope Display System -Tablet (EDS 500); MiiS Horus Endoscope Display System -Video Box (EVS 700)
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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.