TRI-FLOW THREE WAY STOPCOCK— 510(k) K961982

Substantially Equivalent

North, Inc.

FDA 510(k) clearance K961982 for TRI-FLOW THREE WAY STOPCOCK, Substantially Equivalent on 1997-02-21. Applicant: North, Inc..

Clearance details

Applicant: North, Inc.
Product code: Code FMG
Advisory panel: General Hospital
Date received: 1996-05-20
Decision date: 1997-02-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Northfield, MN, US

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Adverse events under product code FMG

product code FMG

Death: 14
Malfunction: 3,433
Other: 1
Total: 3,448

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.