MED-NET STOPCOCKS— 510(k) K955782

Name: FDA 510(k) clearance K955782
Creator: U.S. Food and Drug Administration
Published: 1996-02-21

Substantially Equivalent

Mednet, Inc.

FDA 510(k) clearance K955782 for MED-NET STOPCOCKS, Substantially Equivalent on 1996-02-21. Applicant: Mednet, Inc.. Device class: 2.

Clearance details

Applicant: Mednet, Inc.
Product code: Code FMG
Device class: Class 2
Regulation: 21 CFR 880.5440
Advisory panel: General Hospital
Date received: 1995-12-21
Decision date: 1996-02-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sunland, CA, US

Download summary PDF View on FDA.gov ↗

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K862887 — UPHOLSTERED BUCKET SEAT1986-08-14
K862892 — CASTER CAR1986-08-14
K862886 — KOOYCHAIR (PEDIATRIC)1986-08-13

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.