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FDA 510(k)

SYNGO PERFUSION-CT

K-Number: K033832 · 2003-12-23

ApplicantSiemens AG Medical Solutions
Decision Date2003-12-23
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SYNGO PERFUSION-CT 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 2003-12-23 under 510(k) number K033832. 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 PERFUSION-CT?

SYNGO PERFUSION-CT is a medical device that received FDA 510(k) clearance on 2003-12-23. The listed applicant is Siemens AG Medical Solutions. The 510(k) number is K033832.

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

SYNGO PERFUSION-CT received FDA 510(k) clearance on 2003-12-23, under 510(k) number K033832.

Who is the listed applicant for SYNGO PERFUSION-CT?

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 PERFUSION-CT?

The FDA product code for SYNGO PERFUSION-CT 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)

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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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