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FDA 510(k)

CARDIAC TAGGING TECHNIQUES/MAGNETOM VISION AND MAGNETOM IMPACT

K-Number: K973799 · 1998-01-02

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1998-01-02
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CARDIAC TAGGING TECHNIQUES/MAGNETOM VISION AND MAGNETOM IMPACT 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 1998-01-02 under 510(k) number K973799. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CARDIAC TAGGING TECHNIQUES/MAGNETOM VISION AND MAGNETOM IMPACT?

CARDIAC TAGGING TECHNIQUES/MAGNETOM VISION AND MAGNETOM IMPACT is a medical device that received FDA 510(k) clearance on 1998-01-02. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K973799.

When did CARDIAC TAGGING TECHNIQUES/MAGNETOM VISION AND MAGNETOM IMPACT receive FDA 510(k) clearance?

CARDIAC TAGGING TECHNIQUES/MAGNETOM VISION AND MAGNETOM IMPACT received FDA 510(k) clearance on 1998-01-02, under 510(k) number K973799.

Who is the listed applicant for CARDIAC TAGGING TECHNIQUES/MAGNETOM VISION AND MAGNETOM IMPACT?

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 CARDIAC TAGGING TECHNIQUES/MAGNETOM VISION AND MAGNETOM IMPACT?

The FDA product code for CARDIAC TAGGING TECHNIQUES/MAGNETOM VISION AND MAGNETOM IMPACT is LNH.

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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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