Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

SYNGO IMAGING CCF VA10A

K-Number: K073418 · 2008-02-29

Decision Date2008-02-29
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SYNGO IMAGING CCF VA10A 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 2008-02-29 under 510(k) number K073418. 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 IMAGING CCF VA10A?

SYNGO IMAGING CCF VA10A is a medical device that received FDA 510(k) clearance on 2008-02-29. The listed applicant is Siemens AG Medical Solutions. The 510(k) number is K073418.

When did SYNGO IMAGING CCF VA10A receive FDA 510(k) clearance?

SYNGO IMAGING CCF VA10A received FDA 510(k) clearance on 2008-02-29, under 510(k) number K073418.

Who is the listed applicant for SYNGO IMAGING CCF VA10A?

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 IMAGING CCF VA10A?

The FDA product code for SYNGO IMAGING CCF VA10A 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 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.

View all 29 devices →

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

View on FDA Database →

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

↑