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/ Sanguina, Inc.
Sanguina, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
1
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K221508
AnemoCheck Home
September 29, 2023
K163215
AnemoCheck
September 13, 2017