ClearanceBrief
510(k) K030544 ยท OWB Interventional Fluoroscopic X-Ray System

RFX FLUROSCOPIC DIGITAL IMAGING SYSTEM

ApplicantSigma Vision, Inc., Rockville MD, US
DecisionSubstantially Equivalent, May 21, 2003
ReceivedFeb 20, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K030544

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.