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FDA 510(k), K181260, MiiS Horus Scope DPT 100
FDA 510(k), K181260, MiiS Horus Scope DPT 100
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510(K) Number: K181260
Device Name: MiiS Horus Scope DPT 100
Manufacturer: Medimaging Integrated Solution Inc. (MiiS)
Device Classification Name: Tonometer, Ac-Powered
Regulation Number: 886.1930
Classification Product Code: HKX
Date Received: 05/11/2018
Decision Date: 06/21/2019
Regulation Medical Specialty: Ophthalmic
Device Name: MiiS Horus Scope DPT 100
Manufacturer: Medimaging Integrated Solution Inc. (MiiS)
Device Classification Name: Tonometer, Ac-Powered
Regulation Number: 886.1930
Classification Product Code: HKX
Date Received: 05/11/2018
Decision Date: 06/21/2019
Regulation Medical Specialty: Ophthalmic
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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