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FDA 510(k)

SYNGO MR 2002B

K-Number: K020991 · 2002-06-13

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2002-06-13
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SYNGO MR 2002B 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 2002-06-13 under 510(k) number K020991. 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 SYNGO MR 2002B?

SYNGO MR 2002B is a medical device that received FDA 510(k) clearance on 2002-06-13. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K020991.

When did SYNGO MR 2002B receive FDA 510(k) clearance?

SYNGO MR 2002B received FDA 510(k) clearance on 2002-06-13, under 510(k) number K020991.

Who is the listed applicant for SYNGO MR 2002B?

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 SYNGO MR 2002B?

The FDA product code for SYNGO MR 2002B 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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