510(k) K193225 · KPR System, X-Ray, Stationary

KDR AU-DDR System Advanced U-Arm with Dynamic Digital Radiography, KDR AU System Advanced U-Arm with Static Digital Radiography

Applicant	Konica Minolta Healthcare Americas, Inc., Garner NC, US
Decision	Substantially Equivalent, Jan 15, 2020
Received	Nov 22, 2019
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K193225

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.