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

DISCOVERY XR656 WITH VOLUMERAD (DIGITAL TOMOSYNTHESIS)

K Number: K132261 · Decision Nov 18, 2013
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
41
Applicant Total
104
Review Days
122

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Basic Information

Device Name
DISCOVERY XR656 WITH VOLUMERAD (DIGITAL TOMOSYNTHESIS)
K Number
K132261
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1740
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ge Medical Systems, LLC
Date Received
July 19, 2013
Decision Date
November 18, 2013
Product Code
IZF
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
IZF System, X-Ray, Tomographic

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