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VesoFlow Lite DVT Compression Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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