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FDA 510(k)

PERFUSION PACKAGE FOR MAGNETOM VISION AND SYMPHONY SYSTEMS

K-Number: K984224 · 1999-02-02

ApplicantSiemens Corp.
Decision Date1999-02-02
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PERFUSION PACKAGE FOR MAGNETOM VISION AND SYMPHONY SYSTEMS is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Corp.. It received FDA 510(k) clearance on 1999-02-02 under 510(k) number K984224. 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 PERFUSION PACKAGE FOR MAGNETOM VISION AND SYMPHONY SYSTEMS?

PERFUSION PACKAGE FOR MAGNETOM VISION AND SYMPHONY SYSTEMS is a medical device that received FDA 510(k) clearance on 1999-02-02. The listed applicant is Siemens Corp.. The 510(k) number is K984224.

When did PERFUSION PACKAGE FOR MAGNETOM VISION AND SYMPHONY SYSTEMS receive FDA 510(k) clearance?

PERFUSION PACKAGE FOR MAGNETOM VISION AND SYMPHONY SYSTEMS received FDA 510(k) clearance on 1999-02-02, under 510(k) number K984224.

Who is the listed applicant for PERFUSION PACKAGE FOR MAGNETOM VISION AND SYMPHONY SYSTEMS?

The FDA 510(k) record lists Siemens Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PERFUSION PACKAGE FOR MAGNETOM VISION AND SYMPHONY SYSTEMS?

The FDA product code for PERFUSION PACKAGE FOR MAGNETOM VISION AND SYMPHONY 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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