ClearanceBrief
510(k) K093092 ยท DQK Computer, Diagnostic, Programmable

ODYSSEY WORKSTATION

ApplicantStereotaxis, Inc., St. Louis MO, US
DecisionSubstantially Equivalent, Jan 21, 2010
ReceivedOct 1, 2009
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K093092

No recall in the FDA data names this 510(k).

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