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

PHILIPS VIEWFORUM 2003

K Number: K032096 · Decision Jul 18, 2003
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
97
Review Days
10

Basic Information

Device Name
PHILIPS VIEWFORUM 2003
K Number
K032096
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
PHILIPS MEDICAL SYSTEMS
Date Received
July 8, 2003
Decision Date
July 18, 2003
Product Code
LLZ
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
Y

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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