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Flexitouch Plus System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K203178
510(k) Type
Traditional
Applicant
Tactile Systems Technology, Inc. (DBA Tactile Medical)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/2020
Days to Decision
55 days
Submission Type
Summary

Flexitouch Plus System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K203178
510(k) Type
Traditional
Applicant
Tactile Systems Technology, Inc. (DBA Tactile Medical)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/2020
Days to Decision
55 days
Submission Type
Summary