ClearanceBrief
510(k) K923049 ยท OWB Interventional Fluoroscopic X-Ray System

UROSKOP D1, UROSKOP D2, AND UROSKOP D3

ApplicantSiemens Medical Solutions USA, Inc., Iselin NJ, US
DecisionSubstantially Equivalent, Sep 15, 1992
ReceivedJun 24, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K923049

DateFirm and productCodeLinked 510(k)
Oct 15, 2003Siemens Medical Solutions USA, Inc
Urology X-Ray System, Uroskop D1/D2/D3 - Hardware for Motor Drive
Terminated
JAANone listed
Jan 30, 2003Siemens Medical Systems Inc
Uroskop D1/D2/D3 - Table, Radiographic, Stationary Top.
Terminated
IXRNone listed

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