Class Class II

BIOMONITOR IV (K230375)

K230375 2023-05-19 Traditional
Home/ Devices/ BIOMONITOR IV (K230375)

Description

BIOMONITOR IV by Biotronik, Inc. — FDA 510(k) cleared cardiovascular device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK230375
Clearance Date2023-05-19
Clearance TypeTraditional
Product CodeMXD
Regulation Number870.1025

Categories

Need More Information?

Contact the manufacturer or request a quote for this device.

Request Quote
Scroll to Top