FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

DIGITAL LIGHTBOX

K Number: K080608 · Decision Apr 17, 2008
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
24
Review Days
44

Basic Information

Device Name
DIGITAL LIGHTBOX
K Number
K080608
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
BRAINLAB, AG
Date Received
March 4, 2008
Decision Date
April 17, 2008
Product Code
LLZ
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LLZ System, Image Processing, Radiological

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