ESTECH ARTERIAL REMOTE ACCESS PERFUSION CANNULA— 510(k) K990573

Substantially Equivalent

Estech, Inc.

FDA 510(k) clearance K990573 for ESTECH ARTERIAL REMOTE ACCESS PERFUSION CANNULA, Substantially Equivalent on 1999-03-11. Applicant: Estech, Inc..

Clearance details

Applicant: Estech, Inc.
Product code: Code DXC
Advisory panel: Cardiovascular
Date received: 1999-02-23
Decision date: 1999-03-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Danville, CA, US

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Adverse events under product code DXC

product code DXC

Death: 14
Injury: 442
Malfunction: 2,209
Other: 1
Total: 2,666

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.