PERCUTANEOUS ARTERIAL/VENOUS CANNULA PLACEMENT KIT— 510(k) K875353

Substantially Equivalent

Dlp, Inc.

FDA 510(k) clearance K875353 for PERCUTANEOUS ARTERIAL/VENOUS CANNULA PLACEMENT KIT, Substantially Equivalent on 1988-03-22. Applicant: Dlp, Inc..

Clearance details

Applicant: Dlp, Inc.
Product code: Code DWF
Advisory panel: Cardiovascular
Date received: 1987-12-31
Decision date: 1988-03-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Grand Rapids, MI, US

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Adverse events under product code DWF

product code DWF

Death: 106
Injury: 386
Malfunction: 2,323
Total: 2,815

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.