Cardiacassist, Inc.
Cardiacassist, Inc. holds FDA 510(k) medical device clearances, first cleared 2000, most recent 2024.
Top product codes for Cardiacassist, Inc.
Recent clearances by Cardiacassist, Inc.
- K233736 — LifeSPARC System
- K232480 — ProtekDuo Veno-Venous Cannula Sets
- K232132 — LifeSPARC System
- K211830 — LifeSPARC System
- K202751 — TandemHeart Pump and Escort Controller
- K183623 — LifeSPARC Pump, LifeSPARC Controller
- K181150 — ProtekDuo Mini Veno-Venous Cannula Set
- K162181 — Protek Duo Venous Dilator Set, Protek Solo Venous Dilator Set
- K162214 — Protek Solo 24 Fr Venous Cannula Set
- K160257 — PROTEK Duo 31 Fr. Veno-Venous Cannula Set
- K153295 — TandemLung Oxygenator
- K140999 — TANDEMHEART VENO-VENOUS CANNULA
- K133293 — 15 FR. TANDEMHEART ARTERIAL CANNULA
- K133236 — TANDEMHEART FEMORAL VENOUS CANNULA SET
- K120543 — TANDEMHEART FEMORAL ARTERIAL CANNULA SET
- K110493 — TANDEMHEART PUMP
- K082425 — TANDEMHEART TRANSSEPTAL CANNULA- EF 72
- K061369 — TANDEM HEART ESCORT (T.H.E.) CONTROLLER, MODEL 5140-8500
- K052570 — TANDEMHEART TRANSSEPTAL CANNULA SET-EF, MODEL 5140-6221
- K030398 — CARDIACASSIST TRANSSEPTAL CANNULA SET, MODEL 5132-6221
- K991783 — AB-180 XC SYSTEM, MODEL AB-180XC
Data sourced from openFDA. This site is unofficial and independent of the FDA.