WIRELESS MONITORING SYSTEM— 510(k) K110809

Substantially Equivalent

Carefusion 303, Inc.

FDA 510(k) clearance K110809 for WIRELESS MONITORING SYSTEM, Substantially Equivalent on 2011-07-05. Applicant: Carefusion 303, Inc..

Clearance details

Applicant: Carefusion 303, Inc.
Product code: Code DRG
Advisory panel: Cardiovascular
Date received: 2011-03-23
Decision date: 2011-07-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Abingdon,Oxon, GB

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Adverse events under product code DRG

product code DRG

Death: 5
Total: 5

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.