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

ENSITE VERISMO SEGMENTATION TOOL V.2.0

K Number: K101697 · Decision Sep 22, 2010
Classifications
1
FEI Numbers
599
Registration Numbers
599
Same Product Code
2271
Applicant Total
105
Review Days
98

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Basic Information

Device Name
ENSITE VERISMO SEGMENTATION TOOL V.2.0
K Number
K101697
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
St Jude Medical
Date Received
June 16, 2010
Decision Date
September 22, 2010
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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