LIFESITE HEMODIALYSIS ACCESS SYSTEM/CANNULA EXCHANGE, MODEL LHAS14120 & LHCEK0000— 510(k) K001633

Substantially Equivalent

Vasca, Inc.

FDA 510(k) clearance K001633 for LIFESITE HEMODIALYSIS ACCESS SYSTEM/CANNULA EXCHANGE, MODEL LHAS14120 & LHCEK0000, Substantially Equivalent on 2000-08-24. Applicant: Vasca, Inc..

Clearance details

Applicant: Vasca, Inc.
Product code: Code MSD
Advisory panel: Gastroenterology, Urology
Date received: 2000-05-26
Decision date: 2000-08-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tewksburt, MA, US

Download summary PDF View on FDA.gov ↗

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.