Somatom Definition

FDA 510(k) K052216 · Siemens Medical Systems, Inc.

Substantially Equivalent

510(k) numberK052216

Submission

Device name
Somatom Definition
Applicant
Siemens Medical Systems, Inc.
Mavern, PA, US
Received
August 3, 2005
Decision date
September 8, 2005
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
JAK – System, X-Ray, Tomography, Computed
Device class
Class II (moderate risk)
Regulation
21 CFR 892.1750
Specialty
Radiology

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More from Siemens Medical Solutions USA, Inc.

510(k)DeviceDecision
K133646AdmireJAK · Traditional 06/20/2014SE
K130901Somatom Definition AS OpenJAK · Traditional 01/02/2014SE
K123540Syngo CT Pulmo 3DJAK · Traditional 08/29/2013SE
K123541Syngo.Ct Neuro PerfusionJAK · Traditional 04/02/2013SE
K122909Syngo Single Source Dual EngeryJAK · Traditional 12/27/2012SE
K122471Somatom DefinitionJAK · Special 09/11/2012SE
K120579Somatom Definition EdgeJAK · Special 05/23/2012SE
K121072Somatom Definition FlashJAK · Special 05/08/2012SE
K113342Somatom Definition FlashJAK · Traditional 12/29/2011SE
K051602Axiom Sireskop SDJAA · Traditional 07/07/2005SE

Questions and answers

When was Somatom Definition cleared by the FDA?

Somatom Definition (K052216) received a 510(k) decision of Substantially Equivalent on September 8, 2005, 36 days after the submission was received.

What is the product code of K052216?

The FDA product code is JAK – System, X-Ray, Tomography, Computed, a Class II (moderate risk) device regulated under 21 CFR 892.1750.