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FDA 510(k)

SYNGO TRUED, MODEL VC10A

K-Number: K061671 · 2006-06-29

Decision Date2006-06-29
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SYNGO TRUED, MODEL VC10A 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 2006-06-29 under 510(k) number K061671. 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 TRUED, MODEL VC10A?

SYNGO TRUED, MODEL VC10A is a medical device that received FDA 510(k) clearance on 2006-06-29. The listed applicant is Siemens Medical Solutions. The 510(k) number is K061671.

When did SYNGO TRUED, MODEL VC10A receive FDA 510(k) clearance?

SYNGO TRUED, MODEL VC10A received FDA 510(k) clearance on 2006-06-29, under 510(k) number K061671.

Who is the listed applicant for SYNGO TRUED, MODEL VC10A?

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 TRUED, MODEL VC10A?

The FDA product code for SYNGO TRUED, MODEL VC10A is LLZ.

Related Clinical Trials

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.

Other records listing Siemens 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.

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Related Devices (Code: LLZ)

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.

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.

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