ClearanceBrief
510(k) K940484 ยท IZI System, X-Ray, Angiographic

COROSKOP HI-P ANGIOGRAPHIC X-RAY SYSTEM

ApplicantSiemens Medical Solutions USA, Inc., Iselin NJ, US
DecisionSubstantially Equivalent, Apr 19, 1994
ReceivedFeb 2, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K940484

DateFirm and productCodeLinked 510(k)
Nov 4, 2008Siemens Medical Solutions USA, Inc
Coroskop X-Ray System, Model numbers 6258219 and 6379759.
Terminated
IZINone listed
Nov 4, 2008Siemens Medical Solutions USA, Inc
Bicor X-Ray System, Model number 9023136.
Terminated
IZINone listed
Nov 4, 2008Siemens Medical Solutions USA, Inc
Bicor Hi-P X-Ray System, Model numbers 6379767 and 6258383.
Terminated
IZINone listed
Nov 4, 2008Siemens Medical Solutions USA, Inc
Coroskop Top X-Ray System, Model number 6134808.
Terminated
IZINone listed
Nov 4, 2008Siemens Medical Solutions USA, Inc
Coroskop C X-Ray System, Model numbers 6005636 and 9108572.
Terminated
IZINone listed
Nov 4, 2008Siemens Medical Solutions USA, Inc
BICOR HS X-Ray System, Model number 6005776
Terminated
IZINone listed
Nov 4, 2008Siemens Medical Solutions USA, Inc
COROSKOP HS-ACS X-Ray System, Model number 6134659.
Terminated
IZINone listed
Nov 4, 2008Siemens Medical Solutions USA, Inc
BICOR POLYDOROS X-Ray System, Model number 6134667.
Terminated
IZINone listed
Nov 4, 2008Siemens Medical Solutions USA, Inc
BICOR TOP X-Ray System, Model number 6134816.
Terminated
IZINone listed

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