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FDA 510(k)

ACTIVE ECG ELECTRODES MAGNETOM VISION SYSTEMS

K-Number: K983327 · 1998-10-09

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1998-10-09
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ACTIVE ECG ELECTRODES MAGNETOM VISION SYSTEMS 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 1998-10-09 under 510(k) number K983327. 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 ACTIVE ECG ELECTRODES MAGNETOM VISION SYSTEMS?

ACTIVE ECG ELECTRODES MAGNETOM VISION SYSTEMS is a medical device that received FDA 510(k) clearance on 1998-10-09. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K983327.

When did ACTIVE ECG ELECTRODES MAGNETOM VISION SYSTEMS receive FDA 510(k) clearance?

ACTIVE ECG ELECTRODES MAGNETOM VISION SYSTEMS received FDA 510(k) clearance on 1998-10-09, under 510(k) number K983327.

Who is the listed applicant for ACTIVE ECG ELECTRODES MAGNETOM VISION SYSTEMS?

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 ACTIVE ECG ELECTRODES MAGNETOM VISION SYSTEMS?

The FDA product code for ACTIVE ECG ELECTRODES MAGNETOM VISION SYSTEMS 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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