510(k) K013641 · GEI Electrosurgical, Cutting & Coagulation & Accessories

SENORX BIOPSY DEVICE, DRIVER, CONTROL MODULE, INCLUDING ACCESSORIES (POWER CORD,CONNECTOR CORDS AND FOOTSWITCH), VACUUMS

Applicant	Senorx, Inc., Aliso Viejo CA, US
Decision	Substantially Equivalent, Jan 29, 2002
Received	Nov 5, 2001
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K013641

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.