ClearanceBrief
510(k) K941611 ยท JAA System, X-Ray, Fluoroscopic, Image-Intensified

TDA-4000/A4

ApplicantToshiba America Medical Systems, In.C, Tustin CA, US
DecisionSubstantially Equivalent, May 13, 1994
ReceivedApr 4, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K941611

DateFirm and productCodeLinked 510(k)
Nov 6, 2003Toshiba American Med Sys Inc
Digital Fluorographic System model DFP-2000A.
Terminated
JAANone listed

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