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

Name: FDA 510(k) clearance K961982
Creator: U.S. Food and Drug Administration
Published: 1997-02-21

Substantially Equivalent

North, Inc.

FDA 510(k) clearance K961982 for TRI-FLOW THREE WAY STOPCOCK, Substantially Equivalent on 1997-02-21. Applicant: North, Inc.. Device class: 2.

Clearance details

Applicant: North, Inc.
Product code: Code FMG
Device class: Class 2
Regulation: 21 CFR 880.5440
Advisory panel: General Hospital
Date received: 1996-05-20
Decision date: 1997-02-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Northfield, MN, US

Download summary PDF View on FDA.gov ↗

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K223175 — lntravascular Administration Sets with Stopcock and Manifold2023-03-10
K211204 — SafePort(TM) Manifold (or Stopcock)2022-09-15
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K954189 — EASI-JECTOR CONTROL SYSTEM1995-10-19

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.