FDA grants 510(k) clearance for Urolution Medical’s OpenFlo catheter

Urolution Medical is preparing comparative clinical trials to evaluate catheter performance and patient outcomes.

The US Food and Drug Administration (FDA) has granted 510(k) clearance for Urolution Medical’s OpenFlo urinary catheter.

Cleared for adult use, the device drains the urinary tract and can remain in place for up to 30 days.

Following the clearance, Urolution Medical is preparing comparative clinical trials to evaluate the catheter performance and patient outcomes.

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