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FDA 510(k)

DCA VANTAGE, MODEL 5075

K-Number: K071466 · 2007-10-09

Decision Date2007-10-09
Product CodeLCP
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

DCA VANTAGE, MODEL 5075 is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Solutions Diagnostics. It received FDA 510(k) clearance on 2007-10-09 under 510(k) number K071466. The device is classified under product code LCP. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DCA VANTAGE, MODEL 5075?

DCA VANTAGE, MODEL 5075 is a medical device that received FDA 510(k) clearance on 2007-10-09. The listed applicant is Siemens Medical Solutions Diagnostics. The 510(k) number is K071466.

When did DCA VANTAGE, MODEL 5075 receive FDA 510(k) clearance?

DCA VANTAGE, MODEL 5075 received FDA 510(k) clearance on 2007-10-09, under 510(k) number K071466.

Who is the listed applicant for DCA VANTAGE, MODEL 5075?

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

What is the FDA product code for DCA VANTAGE, MODEL 5075?

The FDA product code for DCA VANTAGE, MODEL 5075 is LCP.

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 Diagnostics 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 11 devices →

Related Devices (Code: LCP)

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.

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