510(k) K213466 · DQY Catheter, Percutaneous

Houdini Cross Support Catheter

Applicant	Cruzar Medsystems, Inc., Braintree MA, US
Decision	Substantially Equivalent, Oct 20, 2022
Received	Oct 28, 2021
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K213466

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.