I.V. FILTER-PREVENT— 510(k) K813454

Substantially Equivalent

Pioneer Viggo, Inc.

FDA 510(k) clearance K813454 for I.V. FILTER-PREVENT, Substantially Equivalent on 1982-01-05. Applicant: Pioneer Viggo, Inc..

Clearance details

Applicant: Pioneer Viggo, Inc.
Product code: Code FPB
Advisory panel: General Hospital
Date received: 1981-12-10
Decision date: 1982-01-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code FPB

product code FPB

Other: 1
Total: 1

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.