FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

DICOM THEATER

K Number: K033153 · Decision Apr 23, 2004
Classifications
1
FEI Numbers
599
Registration Numbers
599
Same Product Code
2271
Applicant Total
57
Review Days
206

Basic Information

Device Name
DICOM THEATER
K Number
K033153
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ferguson Medical
Date Received
September 30, 2003
Decision Date
April 23, 2004
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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