HEMOSTATIC SIDE-ARM ADAPTER— 510(k) K813578

Substantially Equivalent

Advanced Catheter Systems

FDA 510(k) clearance K813578 for HEMOSTATIC SIDE-ARM ADAPTER, Substantially Equivalent on 1982-01-18. Applicant: Advanced Catheter Systems.

Clearance details

Applicant: Advanced Catheter Systems
Product code: Code DYG
Advisory panel: Cardiovascular
Date received: 1981-12-23
Decision date: 1982-01-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code DYG

product code DYG

Death: 18
Malfunction: 1,051
Other: 1
Total: 1,070

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.