510(k) K232910

Device
CombiDiagnost R90
Applicant
Philips Medical Systems Dmc GmbH
510(k) number
K232910
Product code
JAA
Decision
Substantially Equivalent (SESE)
Decision date
2023-10-19
Date received
2023-09-19
Regulation
892.1650
Classification name
System, X-Ray, Fluoroscopic, Image-Intensified
Medical specialty
Radiology
Review panel
Radiology
Device class
2
Clearance type
Special
Statement or summary
Summary
Third party reviewed
N

Related Records

Applicant Contact

Contact
Ming Xiao
Address
Röntgenstrasse 24 Hamburg DE 22335 22335

FDA Registration Numbers

Source Documents

510(k) summary PDF

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