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Catheter, Pressure Monitoring, Cardiac

FDA product code OBI · Class 2 · Cardiovascular

50

Registered devices

22

Adverse events

1

Recalls

1

510(k) clearances

Devices with this code

RXi® Cable — ACIST MEDICAL SYSTEMS, INC.RXi® Cable — ACIST MEDICAL SYSTEMS, INC.RXi® Cable — ACIST MEDICAL SYSTEMS, INC.ACIST RXi® Cart — ACIST MEDICAL SYSTEMS, INC.RXi® Cable — ACIST MEDICAL SYSTEMS, INC.RXi® Cable — ACIST MEDICAL SYSTEMS, INC.RXi® Cable — ACIST MEDICAL SYSTEMS, INC.RXi® Cable — ACIST MEDICAL SYSTEMS, INC.ACIST RXi® System and Accessories — ACIST MEDICAL SYSTEMS, INC.RXi® Cable — ACIST MEDICAL SYSTEMS, INC.RXi® Cable — ACIST MEDICAL SYSTEMS, INC.RXi® Cable — ACIST MEDICAL SYSTEMS, INC.ACIST Navvus®II Catheter — ACIST MEDICAL SYSTEMS, INC.ACIST RXi® System — ACIST MEDICAL SYSTEMS, INC.ACIST RXi® System — ACIST MEDICAL SYSTEMS, INC.RXi® Console Cable — ACIST MEDICAL SYSTEMS, INC.RXi® Cable — ACIST MEDICAL SYSTEMS, INC.RXi® Cable — ACIST MEDICAL SYSTEMS, INC.ACIST Navvus®II Catheter — ACIST MEDICAL SYSTEMS, INC.RXi® Cable — ACIST MEDICAL SYSTEMS, INC.RXi® Cable — ACIST MEDICAL SYSTEMS, INC.ACIST RXi® System and Accessories — ACIST MEDICAL SYSTEMS, INC.RXi® Cable — ACIST MEDICAL SYSTEMS, INC.RXi® Cable — ACIST MEDICAL SYSTEMS, INC.

Recent recalls

Date	Firm	Reason
2014-03-13	Merit Medical Systems, Inc.	The products are labeled as sterile but were not sterilized.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.