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FDA 510(k)

SYNGO DYNAMICS VERSION 7.0

K-Number: K081018 · 2008-04-25

ApplicantSiemens Medical Solutions
Decision Date2008-04-25
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SYNGO DYNAMICS VERSION 7.0 is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Solutions. It received FDA 510(k) clearance on 2008-04-25 under 510(k) number K081018. 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 7.0?

SYNGO DYNAMICS VERSION 7.0 is a medical device that received FDA 510(k) clearance on 2008-04-25. The listed applicant is Siemens Medical Solutions. The 510(k) number is K081018.

When did SYNGO DYNAMICS VERSION 7.0 receive FDA 510(k) clearance?

SYNGO DYNAMICS VERSION 7.0 received FDA 510(k) clearance on 2008-04-25, under 510(k) number K081018.

Who is the listed applicant for SYNGO DYNAMICS VERSION 7.0?

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

What is the FDA product code for SYNGO DYNAMICS VERSION 7.0?

The FDA product code for SYNGO DYNAMICS VERSION 7.0 is LLZ.

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Other records listing Siemens Medical Solutions as applicant

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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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