510(k) K222195

Device
aprevo® Digital Workflow
Applicant
Carlsmed, Inc.
510(k) number
K222195
Product code
LLZ
Decision
Substantially Equivalent (SESE)
Decision date
2022-12-30
Date received
2022-07-22
Regulation
892.2050
Classification name
System, Image Processing, Radiological
Medical specialty
Radiology
Review panel
Radiology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
Karen Liu
Address
1800 Aston Ave. Suite 100 Carlsbad CA US 92008 92008

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON

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