DERMAPORT PERCUTANEOUS VASCULAR ACCESS SYSTEM (PVAS)— 510(k) K071202

Unknown

Dermaport, Inc.

FDA 510(k) clearance K071202 for DERMAPORT PERCUTANEOUS VASCULAR ACCESS SYSTEM (PVAS), Unknown on 2007-11-30. Applicant: Dermaport, Inc..

Clearance details

Applicant: Dermaport, Inc.
Product code: Code MSD
Advisory panel: Gastroenterology, Urology
Date received: 2007-05-01
Decision date: 2007-11-30
Decision: Unknown
Clearance type: Abbreviated
Location: Stoughton, WI, US

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Adverse events under product code MSD

product code MSD

Death: 67
Injury: 545
Malfunction: 3,661
Total: 4,273

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.