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FDA 510(k)

SYNGO NEURO DSA CT

K-Number: K053024 · 2005-11-04

ApplicantSiemens AG
Decision Date2005-11-04
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SYNGO NEURO DSA CT is the device name listed in this FDA 510(k) record. The listed applicant is Siemens AG. It received FDA 510(k) clearance on 2005-11-04 under 510(k) number K053024. 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 NEURO DSA CT?

SYNGO NEURO DSA CT is a medical device that received FDA 510(k) clearance on 2005-11-04. The listed applicant is Siemens AG. The 510(k) number is K053024.

When did SYNGO NEURO DSA CT receive FDA 510(k) clearance?

SYNGO NEURO DSA CT received FDA 510(k) clearance on 2005-11-04, under 510(k) number K053024.

Who is the listed applicant for SYNGO NEURO DSA CT?

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

What is the FDA product code for SYNGO NEURO DSA CT?

The FDA product code for SYNGO NEURO DSA CT is JAK.

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Other records listing Siemens AG 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.

K123375SYNGO.VIAK110366SYNGO.CT CARDIAC FUNCTIONK071310SYNGO CT ONCOLOGY SOFTWARE PACKAGEK063507SYNGO NEURO PBV CTK063373FLEX LOOP COIL SET 3TK050867SYNGO BODY PERFUSION-CT

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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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