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FDA 510(k)

LUNGCARE CT SOFTWARE PACKAGE

K-Number: K022013 · 2002-07-16

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2002-07-16
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

LUNGCARE CT SOFTWARE PACKAGE 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 2002-07-16 under 510(k) number K022013. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LUNGCARE CT SOFTWARE PACKAGE?

LUNGCARE CT SOFTWARE PACKAGE is a medical device that received FDA 510(k) clearance on 2002-07-16. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K022013.

When did LUNGCARE CT SOFTWARE PACKAGE receive FDA 510(k) clearance?

LUNGCARE CT SOFTWARE PACKAGE received FDA 510(k) clearance on 2002-07-16, under 510(k) number K022013.

Who is the listed applicant for LUNGCARE CT SOFTWARE PACKAGE?

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 LUNGCARE CT SOFTWARE PACKAGE?

The FDA product code for LUNGCARE CT SOFTWARE PACKAGE is JAK.

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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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