VASCUCARE ANGIOPUMP— 510(k) K881780

Substantially Equivalent

Vascucare, Inc.

FDA 510(k) clearance K881780 for VASCUCARE ANGIOPUMP, Substantially Equivalent on 1988-09-28. Applicant: Vascucare, Inc..

Clearance details

Applicant: Vascucare, Inc.
Product code: Code DWB
Advisory panel: Cardiovascular
Date received: 1988-04-26
Decision date: 1988-09-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Orangeburg, NY, US

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Adverse events under product code DWB

product code DWB

Death: 2
Total: 2

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.