V-2200 INFANT INCUBATOR— 510(k) K061280

Name: FDA 510(k) clearance K061280
Creator: U.S. Food and Drug Administration
Published: 2006-06-27

Substantially Equivalent

Neoforce Group, Inc.

FDA 510(k) clearance K061280 for V-2200 INFANT INCUBATOR, Substantially Equivalent on 2006-06-27. Applicant: Neoforce Group, Inc.. Device class: 2.

Clearance details

Applicant: Neoforce Group, Inc.
Product code: Code FMZ
Device class: Class 2
Regulation: 21 CFR 880.5400
Advisory panel: General Hospital
Date received: 2006-05-08
Decision date: 2006-06-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Doylestown, PA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code FMZ

product code FMZ

Death: 2
Malfunction: 457
Other: 1
Total: 460

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.