ACIST GENTOO CONTRAST INJECTION SYSTEM— 510(k) K020892

Substantially Equivalent

Acist Medical Systems

FDA 510(k) clearance K020892 for ACIST GENTOO CONTRAST INJECTION SYSTEM, Substantially Equivalent on 2003-01-27. Applicant: Acist Medical Systems.

Clearance details

Applicant: Acist Medical Systems
Product code: Code DXT
Advisory panel: Cardiovascular
Date received: 2002-03-19
Decision date: 2003-01-27
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Eden Prairie, MN, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code DXT

product code DXT

Death: 39
Injury: 242
Malfunction: 463
Other: 3
Total: 747

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

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