Lumend, Inc.

11FDA 510(k) medical device clearances.

Top product codes for Lumend, Inc.

DQY — Cardiovascular8 devices
PDU — Cardiovascular3 devices

Recent clearances by Lumend, Inc.

K043534 — MODIFICATION TO OUTBACK CATHETERCode DQY·2005-01-21
K040771 — MODIFICATION TO OUTBACK CATHETERCode DQY·2004-04-23
K033535 — LUMEND FRONTRUNNER CTO CATHETER AND ACCESSORIESCode PDU·2004-01-07
K032298 — MODIFICATION TO OUTBACK CATHETERCode DQY·2003-08-26
K031005 — LUMEND FRONTRUNNER GW CTO CATHETERCode PDU·2003-06-18
K023114 — LUMEND FRONTRUNNER CTO CATHETERCode PDU·2003-01-23
K023223 — MODIFICATION TO LUMEND FRONTRUNNER CTO CATHETERCode DQY·2002-10-24
K013284 — LUMEND FRONTRUNNER CTO CORONARY CATHETERCode DQY·2002-02-11
K011562 — LUMEND PERCUTANEOUS CATHETERCode DQY·2002-01-16
K014117 — MODIFICATION TO OUTBACK CATHETERCode DQY·2002-01-11
K001577 — OUTBACK CATHETERCode DQY·2001-01-11

Data sourced from openFDA. This site is unofficial and independent of the FDA.