510(k) K945459 · IZI System, X-Ray, Angiographic

DLX

Applicant	General Electric Co., Milwaukee WI, US
Decision	Substantially Equivalent, Jan 30, 1995
Received	Nov 7, 1994
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K945459

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.