FDA 510(k) Applications Submitted by Scopis GmbH
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K171661 | 06/05/2017 | Scopis Extended Instrument Set EM | Scopis GmbH |
| K161491 | 06/01/2016 | Scopis Hybrid Navigation System EM | Scopis GmbH |
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