Class Class II

OmniTom Elite (K223447)

K223447 2023-06-01 Traditional
Home/ Devices/ OmniTom Elite (K223447)

Description

OmniTom Elite by Neurologica Corporation, A Subsidiary of Samsung — FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK223447
Clearance Date2023-06-01
Clearance TypeTraditional
Product CodeJAK
Regulation Number892.1750

Categories

Need More Information?

Contact the manufacturer or request a quote for this device.

Request Quote
Scroll to Top