510(k) K080637 · DQX Wire, Guide, Catheter

POWERASSET RADIOFREQUENCY GUIDWIRE, MODEL VARIOUS

Applicant	Stereotaxis, Inc., St. Louis MO, US
Decision	Substantially Equivalent, Aug 12, 2008
Received	Mar 6, 2008
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K080637

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.