St Jude Medical
St Jude Medical holds FDA 510(k) medical device clearances, first cleared 2000, most recent 2018, with 22 FDA device recalls on record.
Clearances by St Jude Medical — page 2
101–105 of 105- K013029 — SEAL-AWAY CS INTRODUCER KIT, MODELS 407514, 407515
- K012922 — ULTRAFLEX EV HEMOSTASIS INTRODUCER
- K011766 — 6F EVALUATOR ELECTROPHYSIOLOGY CATHETER, CRD # 402720,402722; 6F EAVUATOR ELECTROPHYSISOLOGY CATHETER, JSN #402721, 4027
- K003729 — ULTIMUM EV HEMOSTASIS INTRODUCER (14F), ULTIMUM EV HEMOSTASIS INTRODUCER (16F), ULTIMUM EV HEMOSTASIS INTRODUCER (18F),
- K002976 — RESPONSE ELECTROPHYSIOLOGY CATHETER, SUPREME ELECTROPHYSIOLOGY CATHETER, MODEL 401XXX AND 401XXX
Data sourced from openFDA. This site is unofficial and independent of the FDA.