ATRIUM'S HYBRID PTFE— 510(k) K925123

Name: FDA 510(k) clearance K925123
Creator: U.S. Food and Drug Administration
Published: 1993-05-27

Unknown

Atrium Medical Corp.

FDA 510(k) clearance K925123 for ATRIUM'S HYBRID PTFE, Unknown on 1993-05-27. Applicant: Atrium Medical Corp.. Device class: 2.

Clearance details

Applicant: Atrium Medical Corp.
Product code: Code DSY
Device class: Class 2
Regulation: 21 CFR 870.3450
Advisory panel: Cardiovascular
Date received: 1992-10-13
Decision date: 1993-05-27
Decision: Unknown
Clearance type: Traditional
Location: Hollis, NH, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code DSY

product code DSY

Death: 29
Injury: 694
Total: 723

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.