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

SYMBIA.NET, SYMBIA.NET SELECT MODEL 10520828, 10520827

K Number: K100619 · Decision May 7, 2010
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
14
Review Days
64

Basic Information

Device Name
SYMBIA.NET, SYMBIA.NET SELECT MODEL 10520828, 10520827
K Number
K100619
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
SIEMENS MEDICAL SOLUTIONS USA INC.
Date Received
March 4, 2010
Decision Date
May 7, 2010
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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