FDA.report

510(k) K092280

Device
CYPHER DICOM PRINT SOLUTION
Applicant
Virtual Imaging, Inc.
510(k) number
K092280
Product code
LMC
Decision
Substantially Equivalent (SESE)
Decision date
2009-10-16
Date received
2009-07-28
Regulation
892.2040
Classification name
Camera, Multi Format, Radiological
Medical specialty
Radiology
Review panel
Radiology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Related Records

Applicant Contact

Contact
DANIEL KAMM
Address
333 Milford Rd. Deerfield IL US 60015 60015

FDA Registration Numbers

Source Documents

510(k) summary PDF

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