COBE HVR 4000 FILTERED HARDSHELL VENOUS RESERVOIR— 510(k) K984456

Substantially Equivalent

Cobe Cardiovascular, Inc.

FDA 510(k) clearance K984456 for COBE HVR 4000 FILTERED HARDSHELL VENOUS RESERVOIR, Substantially Equivalent on 1999-01-11. Applicant: Cobe Cardiovascular, Inc..

Clearance details

Applicant: Cobe Cardiovascular, Inc.
Product code: Code DTN
Advisory panel: Cardiovascular
Date received: 1998-12-15
Decision date: 1999-01-11
Decision: Substantially Equivalent
Clearance type: Special
Location: Arvada, CO, US

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Adverse events under product code DTN

product code DTN

Death: 3
Total: 3

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.