MEDIAID M960 SERIES, VITAL SIGNS MONITOR AND MEDIAID M900 SERIES, PULSE OXIMETER— 510(k) K071642

Substantially Equivalent

Mediaid, Inc.

FDA 510(k) clearance K071642 for MEDIAID M960 SERIES, VITAL SIGNS MONITOR AND MEDIAID M900 SERIES, PULSE OXIMETER, Substantially Equivalent on 2008-05-02. Applicant: Mediaid, Inc..

Clearance details

Applicant: Mediaid, Inc.
Product code: Code DQA
Advisory panel: Cardiovascular
Date received: 2007-06-18
Decision date: 2008-05-02
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.