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VesoFlow Lite DVT Compression Device

Page Type
Cleared 510(K)
510(k) Number
K181217
510(k) Type
Traditional
Applicant
Caremed Supply, Inc.
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
8/5/2018
Days to Decision
90 days
Submission Type
Summary

VesoFlow Lite DVT Compression Device

Page Type
Cleared 510(K)
510(k) Number
K181217
510(k) Type
Traditional
Applicant
Caremed Supply, Inc.
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
8/5/2018
Days to Decision
90 days
Submission Type
Summary