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FDA 510(k)

INFINITY MICRO2+

K-Number: K012770 · 2002-07-23

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2002-07-23
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

INFINITY MICRO2+ 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 2002-07-23 under 510(k) number K012770. 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 INFINITY MICRO2+?

INFINITY MICRO2+ is a medical device that received FDA 510(k) clearance on 2002-07-23. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K012770.

When did INFINITY MICRO2+ receive FDA 510(k) clearance?

INFINITY MICRO2+ received FDA 510(k) clearance on 2002-07-23, under 510(k) number K012770.

Who is the listed applicant for INFINITY MICRO2+?

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 INFINITY MICRO2+?

The FDA product code for INFINITY MICRO2+ 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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