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FDA 510(k)

SYNGO VOLUME PERFUSION-CT BODY

K-Number: K073373 · 2007-12-18

ApplicantSiemens AG Medical Solutions
Decision Date2007-12-18
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SYNGO VOLUME PERFUSION-CT BODY is the device name listed in this FDA 510(k) record. The listed applicant is Siemens AG Medical Solutions. It received FDA 510(k) clearance on 2007-12-18 under 510(k) number K073373. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYNGO VOLUME PERFUSION-CT BODY?

SYNGO VOLUME PERFUSION-CT BODY is a medical device that received FDA 510(k) clearance on 2007-12-18. The listed applicant is Siemens AG Medical Solutions. The 510(k) number is K073373.

When did SYNGO VOLUME PERFUSION-CT BODY receive FDA 510(k) clearance?

SYNGO VOLUME PERFUSION-CT BODY received FDA 510(k) clearance on 2007-12-18, under 510(k) number K073373.

Who is the listed applicant for SYNGO VOLUME PERFUSION-CT BODY?

The FDA 510(k) record lists Siemens AG Medical Solutions as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SYNGO VOLUME PERFUSION-CT BODY?

The FDA product code for SYNGO VOLUME PERFUSION-CT BODY is JAK.

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Other records listing Siemens AG Medical Solutions as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K123920SYNGO.VIAK120331SYNGO CT DYNAMIC ANGIOK111079SYNGO.VIA WEB VIEWERK101666SYNGO. PLAZA VA20AK100637SYNGO.CT CORONARY ANALYSISK093612SYNGO.PLAZA

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Related Devices (Code: JAK)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261125BodyTom 64 (NL4100); OmniTom Elite (NL5000)Samsung HME America, Inc., dba NeuroLogica Corp.K261229SCENARIA View Phase 6.0Fujifilm CorporationK253836FCT iStream Phase 2Fujifilm CorporationK253450BodyTom Elite (NL4000)NeuroLogica Corp., a Samsung CompanyK253770CardIQ SuiteGE Medical Systems SCSK253560Enhanced Boundary for PCCTGe Medical Systems, LLC

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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