INFUSIONCATH PERIPHERAL INFUSION CATHETER, MODELS VF0012, VF0016, VF0024, VF0028, VF0032, VF0036, VF0040, VF0044— 510(k) K052738

Substantially Equivalent

Veinrx, Inc.

FDA 510(k) clearance K052738 for INFUSIONCATH PERIPHERAL INFUSION CATHETER, MODELS VF0012, VF0016, VF0024, VF0028, VF0032, VF0036, VF0040, VF0044, Substantially Equivalent on 2005-12-06. Applicant: Veinrx, Inc..

Clearance details

Applicant: Veinrx, Inc.
Product code: Code KRA
Advisory panel: Cardiovascular
Date received: 2005-09-30
Decision date: 2005-12-06
Decision: Substantially Equivalent
Clearance type: Special
Location: Miami, FL, US

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Adverse events under product code KRA

product code KRA

Death: 234
Injury: 1,029
Malfunction: 3,012
Other: 2
Total: 4,277

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.