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FDA 510(k)

SOMATOM EMOTION MS

K-Number: K003014 · 2000-10-12

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2000-10-12
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SOMATOM EMOTION MS 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 2000-10-12 under 510(k) number K003014. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SOMATOM EMOTION MS?

SOMATOM EMOTION MS is a medical device that received FDA 510(k) clearance on 2000-10-12. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K003014.

When did SOMATOM EMOTION MS receive FDA 510(k) clearance?

SOMATOM EMOTION MS received FDA 510(k) clearance on 2000-10-12, under 510(k) number K003014.

Who is the listed applicant for SOMATOM EMOTION MS?

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 SOMATOM EMOTION MS?

The FDA product code for SOMATOM EMOTION MS is JAK.

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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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