Acist Medical Systems, Inc.
Acist Medical Systems, Inc. holds FDA 510(k) medical device clearances, first cleared 2001, most recent 2026.
Name variants for Acist Medical Systems, Inc.
as filed with FDA- Acist Medical Systems, Inc.
- ACIST Medical Systems, Inc.
Top product codes for Acist Medical Systems, Inc.
Recent clearances by Acist Medical Systems, Inc.
- K262115 — VueJect® Ultrasound Enhancing Agent Delivery System
- K252638 — VeraPro S100 Multi-Use Syringe (018808) +4 more
- K252653 — ACIST Pro Diagnostic System (019304) +5 more
- 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.