SHILEY FENESTRATED REUSABLE INNER CANNULA, MODIF— 510(k) K930895

Substantially Equivalent

Mallinckrodt Medical Tpi, Inc.

FDA 510(k) clearance K930895 for SHILEY FENESTRATED REUSABLE INNER CANNULA, MODIF, Substantially Equivalent on 1993-07-02. Applicant: Mallinckrodt Medical Tpi, Inc..

Clearance details

Applicant: Mallinckrodt Medical Tpi, Inc.
Product code: Code JOH
Advisory panel: Anesthesiology
Date received: 1993-02-22
Decision date: 1993-07-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Irvine, CA, US

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Adverse events under product code JOH

product code JOH

Death: 42
Injury: 1,344
Malfunction: 5,608
Other: 1
Total: 6,995

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.