BARD(R) WILLIAM HARVEY(R) MACRO FILT CARDIO RESERV— 510(k) K913915

Name: FDA 510(k) clearance K913915
Creator: U.S. Food and Drug Administration
Published: 1992-01-21

Substantially Equivalent

Bard Cardiosurgery Div

FDA 510(k) clearance K913915 for BARD(R) WILLIAM HARVEY(R) MACRO FILT CARDIO RESERV, Substantially Equivalent on 1992-01-21. Applicant: Bard Cardiosurgery Div. Device class: 2.

Clearance details

Applicant: Bard Cardiosurgery Div
Product code: Code DTN
Device class: Class 2
Regulation: 21 CFR 870.4400
Advisory panel: Cardiovascular
Date received: 1991-09-03
Decision date: 1992-01-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tewksbury, MA, US

Download summary PDF View on FDA.gov ↗

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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.