Class Class II

Kosmos (K233826)

K233826 2024-08-29 Traditional
Home/ Devices/ Kosmos (K233826)

Description

Kosmos by EchoNous, Inc. — FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK233826
Clearance Date2024-08-29
Clearance TypeTraditional
Product CodeIYN
Regulation Number892.1550

Categories

Need More Information?

Contact the manufacturer or request a quote for this device.

Request Quote
Scroll to Top