MEDIAID DISPOSABLE NON-ADHESIVE SENSORS, MODEL CST050-2101N; REUSABLE FINGER CLIP SP02 SENSORS, MODEL CST060-2101N— 510(k) K061896

Substantially Equivalent

Mediaid, Inc.

FDA 510(k) clearance K061896 for MEDIAID DISPOSABLE NON-ADHESIVE SENSORS, MODEL CST050-2101N; REUSABLE FINGER CLIP SP02 SENSORS, MODEL CST060-2101N, Substantially Equivalent on 2007-04-12. Applicant: Mediaid, Inc..

Clearance details

Applicant: Mediaid, Inc.
Product code: Code DQA
Advisory panel: Cardiovascular
Date received: 2006-07-03
Decision date: 2007-04-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cerritos, CA, US

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Adverse events under product code DQA

product code DQA

Death: 66
Malfunction: 2,867
Other: 1
Total: 2,934

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.