0.9% SODIUM CHLORIDE VASCULAT ACCESS DEVICE— 510(k) K000632

Substantially Equivalent

Avitro, LLC

FDA 510(k) clearance K000632 for 0.9% SODIUM CHLORIDE VASCULAT ACCESS DEVICE, Substantially Equivalent on 2000-10-19. Applicant: Avitro, LLC.

Clearance details

Applicant: Avitro, LLC
Product code: Code FOZ
Advisory panel: General Hospital
Date received: 2000-02-24
Decision date: 2000-10-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Woodstock, IL, US

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Adverse events under product code FOZ

product code FOZ

Death: 38
Injury: 2,290
Malfunction: 25,858
Other: 11
Total: 28,197

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.