M VISUM ALERT ALARM MANAGEMENT SYSTEM— 510(k) K112282

Substantially Equivalent

Mvisum, Inc.

FDA 510(k) clearance K112282 for M VISUM ALERT ALARM MANAGEMENT SYSTEM, Substantially Equivalent on 2011-11-04. Applicant: Mvisum, Inc..

Clearance details

Applicant: Mvisum, Inc.
Product code: Code MSX
Advisory panel: Cardiovascular
Date received: 2011-08-09
Decision date: 2011-11-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Camden, NJ, US

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Adverse events under product code MSX

product code MSX

Death: 59
Total: 59

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.