510(k) K223766 · OBJ Catheter, Ultrasound, Intravascular

NUVISION NAV Ultrasound Catheter

Applicant	Biosense Webster, Inc., Irvine CA, US
Decision	Substantially Equivalent, Feb 16, 2023
Received	Dec 15, 2022
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K223766

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.