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FDA 510(k)

SIEMENS MICRO2+ WITH VAI SOFTWARE

K-Number: K030640 · 2003-06-03

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2003-06-03
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SIEMENS MICRO2+ WITH VAI SOFTWARE is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2003-06-03 under 510(k) number K030640. The device is classified under product code DQA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIEMENS MICRO2+ WITH VAI SOFTWARE?

SIEMENS MICRO2+ WITH VAI SOFTWARE is a medical device that received FDA 510(k) clearance on 2003-06-03. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K030640.

When did SIEMENS MICRO2+ WITH VAI SOFTWARE receive FDA 510(k) clearance?

SIEMENS MICRO2+ WITH VAI SOFTWARE received FDA 510(k) clearance on 2003-06-03, under 510(k) number K030640.

Who is the listed applicant for SIEMENS MICRO2+ WITH VAI SOFTWARE?

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

What is the FDA product code for SIEMENS MICRO2+ WITH VAI SOFTWARE?

The FDA product code for SIEMENS MICRO2+ WITH VAI SOFTWARE is DQA.

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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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