CIRCUL8 Connect DVT Prevention Device— 510(k) K220761

Substantially Equivalent

Ortho8, Inc.

FDA 510(k) clearance K220761 for CIRCUL8 Connect DVT Prevention Device, Substantially Equivalent on 2022-06-03. Applicant: Ortho8, Inc..

Clearance details

Applicant: Ortho8, Inc.
Product code: Code JOW
Advisory panel: Cardiovascular
Date received: 2022-03-15
Decision date: 2022-06-03
Decision: Substantially Equivalent
Clearance type: Special
Location: Rocklin, CA, US

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