510(k) K223567

Device
CNS-2101 Central Monitor
Applicant
Nihon Kohden Corporation
510(k) number
K223567
Product code
MSX
Decision
Substantially Equivalent (SESE)
Decision date
2023-07-31
Date received
2022-11-29
Regulation
870.2300
Classification name
System, Network And Communication, Physiological Monitors
Medical specialty
Cardiovascular
Review panel
Cardiovascular
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Sandra Gadeyne
Address
1-31-4 Nishiochiai, Shinjuku-Ku Tokyo JP 161-8560 161-8560

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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