NEOPIP INFANT RESUSCITATOR— 510(k) K072021

Substantially Equivalent

Neoforce Group, Inc.

FDA 510(k) clearance K072021 for NEOPIP INFANT RESUSCITATOR, Substantially Equivalent on 2007-09-12. Applicant: Neoforce Group, Inc..

Clearance details

Applicant: Neoforce Group, Inc.
Product code: Code BTM
Advisory panel: Anesthesiology
Date received: 2007-07-23
Decision date: 2007-09-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ivyland, PA, US

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Adverse events under product code BTM

product code BTM

Death: 19
Other: 2
Total: 21

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.