510(k) K222240 · IZI System, X-Ray, Angiographic

EXPLORER AIR® II

Applicant	Surgvision GmbH, Munich, DE
Decision	Substantially Equivalent, Feb 28, 2023
Received	Jul 26, 2022
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K222240

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.