CURBELL PATIENT MONITORING CABLES— 510(k) K081762

Substantially Equivalent

Curbell Electronics, Inc.

FDA 510(k) clearance K081762 for CURBELL PATIENT MONITORING CABLES, Substantially Equivalent on 2008-08-27. Applicant: Curbell Electronics, Inc..

Clearance details

Applicant: Curbell Electronics, Inc.
Product code: Code DSA
Advisory panel: Cardiovascular
Date received: 2008-06-20
Decision date: 2008-08-27
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Greenwood Village, CO, US

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Adverse events under product code DSA

product code DSA

Death: 2
Total: 2

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.