510(k) K241505

Device
DRX-Revolution Mobile X-ray System
Applicant
Carestream Health, Inc.
510(k) number
K241505
Product code
IZL
Decision
Substantially Equivalent (SESE)
Decision date
2024-12-10
Date received
2024-05-28
Regulation
892.1720
Classification name
System, X-Ray, Mobile
Medical specialty
Radiology
Review panel
Radiology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
Gina Maiolo
Address
150 Verona St. Rochester NY US 14608 14608

FDA Registration Numbers

Source Documents

510(k) summary PDF

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