ClearanceBrief
510(k) K802200 ยท KPR System, X-Ray, Stationary

VERTIX 3D-U

ApplicantSiemens Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Oct 23, 1980
ReceivedSep 11, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K802200

DateFirm and productCodeLinked 510(k)
Dec 31, 2005Siemens Medical Solutions USA, Inc
3D TOP Ceiling Stand. X-Ray System model number 8773673
Terminated
IYBNone listed

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