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CIRCUL8 Connect DVT Prevention Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K220761
510(k) Type
Special
Applicant
Ortho8, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/3/2022
Days to Decision
80 days
Submission Type
Statement

CIRCUL8 Connect DVT Prevention Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K220761
510(k) Type
Special
Applicant
Ortho8, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/3/2022
Days to Decision
80 days
Submission Type
Statement