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Apmtd, 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
K230698
Anivia SG1000 Pump Console
April 18, 2023
K221491
Anivia SG1000 Pump Console
February 3, 2023