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FDA 510(k)

SYNGO DYNAMICS, VERSION 5.0

K-Number: K053133 · 2005-12-05

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2005-12-05
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SYNGO DYNAMICS, VERSION 5.0 is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2005-12-05 under 510(k) number K053133. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYNGO DYNAMICS, VERSION 5.0?

SYNGO DYNAMICS, VERSION 5.0 is a medical device that received FDA 510(k) clearance on 2005-12-05. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K053133.

When did SYNGO DYNAMICS, VERSION 5.0 receive FDA 510(k) clearance?

SYNGO DYNAMICS, VERSION 5.0 received FDA 510(k) clearance on 2005-12-05, under 510(k) number K053133.

Who is the listed applicant for SYNGO DYNAMICS, VERSION 5.0?

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

What is the FDA product code for SYNGO DYNAMICS, VERSION 5.0?

The FDA product code for SYNGO DYNAMICS, VERSION 5.0 is LLZ.

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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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