FDA 510(k)

SYNGO CT DYNAMIC ANGIO

K-Number: K120331 · 2012-04-13

Decision Date2012-04-13

Product CodeJAK

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

SYNGO CT DYNAMIC ANGIO 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 2012-04-13 under 510(k) number K120331. 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 CT DYNAMIC ANGIO?

SYNGO CT DYNAMIC ANGIO is a medical device that received FDA 510(k) clearance on 2012-04-13. The listed applicant is Siemens AG Medical Solutions. The 510(k) number is K120331.

When did SYNGO CT DYNAMIC ANGIO receive FDA 510(k) clearance?

SYNGO CT DYNAMIC ANGIO received FDA 510(k) clearance on 2012-04-13, under 510(k) number K120331.

Who is the listed applicant for SYNGO CT DYNAMIC ANGIO?

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 CT DYNAMIC ANGIO?

The FDA product code for SYNGO CT DYNAMIC ANGIO is JAK.

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Official Source

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