DeviceClearance

Product code MSX— Cardiovascular

BeneVision Central Monitoring System

Classification name
System, Network And Communication, Physiological Monitors
Device class
Class 2
Regulation
21 CFR 870.2300
Advisory panel
Cardiovascular
Total cleared
119
First cleared
Most recent

Market context for product code MSX

FDA has cleared 119 devices under product code MSX between 1997 and 2026, filed by 64 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.

Clearances per year

last 15 years

Top applicants under product code MSX

Adverse events under product code MSX

product code MSX
Death
59
Total
59

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Recent clearances under product code MSX

1–100 of 119

Data sourced from openFDA. This site is unofficial and independent of the FDA.