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Scopis GmbH
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K171661
Scopis Extended Instrument Set EM
September 27, 2017
K161491
Scopis Hybrid Navigation System EM
February 9, 2017