SHILEY MULTIPRO CATHETER— 510(k) K832044

Substantially Equivalent

Shiley, Inc.

FDA 510(k) clearance K832044 for SHILEY MULTIPRO CATHETER, Substantially Equivalent on 1983-09-29. Applicant: Shiley, Inc..

Clearance details

Applicant: Shiley, Inc.
Product code: Code DXE
Advisory panel: Cardiovascular
Date received: 1983-06-24
Decision date: 1983-09-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code DXE

product code DXE

Death: 27
Injury: 258
Malfunction: 2,266
Total: 2,551

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.