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

SOMATOM DEFINITION EDGE

K Number: K120579 · Decision May 23, 2012
Classifications
1
FEI Numbers
163
Registration Numbers
163
Same Product Code
818
Applicant Total
25
Review Days
86

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Basic Information

Device Name
SOMATOM DEFINITION EDGE
K Number
K120579
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
892.1750
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Siemens Medical Systems, Inc.
Date Received
February 27, 2012
Decision Date
May 23, 2012
Product Code
JAK
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
JAK System, X-Ray, Tomography, Computed

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Other Clearances by Siemens Medical Systems, Inc.

K Number Device Name
K133646 ADMIRE
K130901 SOMATOM DEFINITION AS OPEN
K123540 SYNGO CT PULMO 3D
K123541 SYNGO.CT NEURO PERFUSION
K122909 SYNGO SINGLE SOURCE DUAL ENGERY
K122471 SOMATOM DEFINITION
K121072 SOMATOM DEFINITION FLASH
K113342 SOMATOM DEFINITION FLASH
K052216 SOMATOM DEFINITION
K051602 AXIOM SIRESKOP SD
Search all 25 clearances from Siemens Medical Systems, Inc. →