510(k) K231870

Device
CASE V7.0 Cardiac Testing System and CardioSoft V7.0 Cardiac Testing System
Applicant
Ge Medical Systems Information Technologies, Inc.
510(k) number
K231870
Product code
DQK
Decision
Substantially Equivalent (SESE)
Decision date
2023-12-13
Date received
2023-06-26
Regulation
870.1425
Classification name
Computer, Diagnostic, Programmable
Medical specialty
Cardiovascular
Review panel
Cardiovascular
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Manjunatha K N
Address
9900 Innovation Dr. Wauwatosa WI US 53226 53226

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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