Acist Medical Systems, Inc.
FDA 510(k) medical device clearances.
Top product codes for Acist Medical Systems, Inc.
Recent clearances by Acist Medical Systems, Inc.
- K233904 — ACIST RXi System (016616); ACIST Navvus II Catheter (016675_
- K203004 — ACIST CVi1 Contrast Delivery System, ACIST CVi Contrast Delivery System
- K193183 — ACIST HDi System, ACIST Kodama Intravascular Ultrasound Catheter
- K190473 — ACIST RXi System and Navvus II Catheter
- K191060 — ACIST CVI1 Contrast Delivery System, A1000 Syringe Kit, A1000V Syringe Kit, BT2000 Manifold Kit, BT2000 Manifold Kit, AngioToiuch Hand Controller Kit
- K191175 — ACIST Kodama Intravascular Ultrasound Catheter, ACIST HDi System
- K171646 — ACISTCVi® Contrast Delivery System
- K173063 — ACIST Kodama Intravascular Ultrasound Catheter, ACIST HDi System
- K172216 — ACIST RXi Mini System
- K093657 — ADAGIO RETRACTING ECG LEAD WIRES
- K052744 — C2000 AUTOMATED MANIFOLD KIT
- K040298 — ACIST ANTIOGRAPHIC INJECTION SYSTEM CONTRAST MANAGEMENT DISPOSABLE KITS
- K012983 — ACIST 4 FRENCH ANGIOGRAPHIC CATHETER
- K010390 — ACIST ANGIOGRAPHIC INJECTION SYSTEM, MODEL R2000-CMS
Data sourced from openFDA. This site is unofficial and independent of the FDA.