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/ Acuvu, Inc.
Acuvu, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K211227
HTx Disposable Hysteroscope System
September 15, 2021
K180096
GDT-1000 System
April 16, 2018