WILLIAM HARVEY VENTED MEDIASTINAL DRAIN— 510(k) K803037

Substantially Equivalent

C.R. Bard, Inc.

FDA 510(k) clearance K803037 for WILLIAM HARVEY VENTED MEDIASTINAL DRAIN, Substantially Equivalent on 1981-02-04. Applicant: C.R. Bard, Inc..

Clearance details

Applicant: C.R. Bard, Inc.
Product code: Code DWM
Advisory panel: Cardiovascular
Date received: 1980-12-01
Decision date: 1981-02-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code DWM

product code DWM

Death: 8
Total: 8

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.