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FDA 510(k)

SIEMENS INFINITY GATEWAY SUITE, MODEL VF2

K-Number: K030657 · 2003-03-21

ApplicantSiemens Medical Solutions
Decision Date2003-03-21
Product CodeMHX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SIEMENS INFINITY GATEWAY SUITE, MODEL VF2 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 2003-03-21 under 510(k) number K030657. The device is classified under product code MHX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIEMENS INFINITY GATEWAY SUITE, MODEL VF2?

SIEMENS INFINITY GATEWAY SUITE, MODEL VF2 is a medical device that received FDA 510(k) clearance on 2003-03-21. The listed applicant is Siemens Medical Solutions. The 510(k) number is K030657.

When did SIEMENS INFINITY GATEWAY SUITE, MODEL VF2 receive FDA 510(k) clearance?

SIEMENS INFINITY GATEWAY SUITE, MODEL VF2 received FDA 510(k) clearance on 2003-03-21, under 510(k) number K030657.

Who is the listed applicant for SIEMENS INFINITY GATEWAY SUITE, MODEL VF2?

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 SIEMENS INFINITY GATEWAY SUITE, MODEL VF2?

The FDA product code for SIEMENS INFINITY GATEWAY SUITE, MODEL VF2 is MHX.

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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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