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FDA 510(k)

MAGNETIC RESONANCE DIAGNOSTIC DEVICE ACCESSORIY

K-Number: K913563 · 1991-09-11

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1991-09-11
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MAGNETIC RESONANCE DIAGNOSTIC DEVICE ACCESSORIY 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 1991-09-11 under 510(k) number K913563. 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 MAGNETIC RESONANCE DIAGNOSTIC DEVICE ACCESSORIY?

MAGNETIC RESONANCE DIAGNOSTIC DEVICE ACCESSORIY is a medical device that received FDA 510(k) clearance on 1991-09-11. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K913563.

When did MAGNETIC RESONANCE DIAGNOSTIC DEVICE ACCESSORIY receive FDA 510(k) clearance?

MAGNETIC RESONANCE DIAGNOSTIC DEVICE ACCESSORIY received FDA 510(k) clearance on 1991-09-11, under 510(k) number K913563.

Who is the listed applicant for MAGNETIC RESONANCE DIAGNOSTIC DEVICE ACCESSORIY?

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 MAGNETIC RESONANCE DIAGNOSTIC DEVICE ACCESSORIY?

The FDA product code for MAGNETIC RESONANCE DIAGNOSTIC DEVICE ACCESSORIY 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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