510(k) K220761 · JOW Sleeve, Limb, Compressible

CIRCUL8 Connect DVT Prevention Device

Applicant	Ortho8, Inc., Rocklin CA, US
Decision	Substantially Equivalent, Jun 3, 2022
Received	Mar 15, 2022
Type	Special
FDA record	Open on fda.gov

Recalls that name K220761

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.