OCCLUSION BALLOON CATHETER, MODEL VENOS— 510(k) K081052

Substantially Equivalent

Oscor, Inc.

FDA 510(k) clearance K081052 for OCCLUSION BALLOON CATHETER, MODEL VENOS, Substantially Equivalent on 2008-06-18. Applicant: Oscor, Inc..

Clearance details

Applicant: Oscor, Inc.
Product code: Code DYG
Advisory panel: Cardiovascular
Date received: 2008-04-14
Decision date: 2008-06-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Palm Harbor, FL, 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.