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CIRCUL8 Connect DVT Prevention Device

Page Type
Cleared 510(K)
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)
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