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

KINETDX

K Number: K041029 · Decision Jul 8, 2004
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
19
Review Days
78

Basic Information

Device Name
KINETDX
K Number
K041029
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
SIEMENS MEDICAL SOLUTIONS, INC.
Date Received
April 21, 2004
Decision Date
July 8, 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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