ClearanceBrief
510(k) K880530 ยท IYB Tube Mount, X-Ray, Diagnostic

CEILING MOUNTED RADIOGRAPHIC SYSTEM TRAUMEX

ApplicantFischer Imaging Corp., Denver CO, US
DecisionSubstantially Equivalent, Mar 3, 1988
ReceivedFeb 9, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K880530

DateFirm and productCodeLinked 510(k)
May 3, 2005Fischer Imaging Corporation
VersaRad Generator
Terminated
IYBNone listed
Jul 20, 2004Fischer Imaging Corporation
VersaRad/Traumex General Radiographic System.
Terminated
IYBNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.