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FDA 510(k)

HIGH ENDS GRADIENTS/MAGNETOM SYMPHONY SYSTEM

K-Number: K991652 · 1999-08-03

ApplicantSiemens Corp.
Decision Date1999-08-03
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

HIGH ENDS GRADIENTS/MAGNETOM SYMPHONY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Corp.. It received FDA 510(k) clearance on 1999-08-03 under 510(k) number K991652. 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 HIGH ENDS GRADIENTS/MAGNETOM SYMPHONY SYSTEM?

HIGH ENDS GRADIENTS/MAGNETOM SYMPHONY SYSTEM is a medical device that received FDA 510(k) clearance on 1999-08-03. The listed applicant is Siemens Corp.. The 510(k) number is K991652.

When did HIGH ENDS GRADIENTS/MAGNETOM SYMPHONY SYSTEM receive FDA 510(k) clearance?

HIGH ENDS GRADIENTS/MAGNETOM SYMPHONY SYSTEM received FDA 510(k) clearance on 1999-08-03, under 510(k) number K991652.

Who is the listed applicant for HIGH ENDS GRADIENTS/MAGNETOM SYMPHONY SYSTEM?

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 HIGH ENDS GRADIENTS/MAGNETOM SYMPHONY SYSTEM?

The FDA product code for HIGH ENDS GRADIENTS/MAGNETOM SYMPHONY SYSTEM 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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