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FDA 510(k)

SOMATOM EXTENDED FIELD OF VIEW SOFTWARE OPTION

K-Number: K032536 · 2003-11-10

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2003-11-10
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SOMATOM EXTENDED FIELD OF VIEW SOFTWARE OPTION 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 2003-11-10 under 510(k) number K032536. 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 EXTENDED FIELD OF VIEW SOFTWARE OPTION?

SOMATOM EXTENDED FIELD OF VIEW SOFTWARE OPTION is a medical device that received FDA 510(k) clearance on 2003-11-10. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K032536.

When did SOMATOM EXTENDED FIELD OF VIEW SOFTWARE OPTION receive FDA 510(k) clearance?

SOMATOM EXTENDED FIELD OF VIEW SOFTWARE OPTION received FDA 510(k) clearance on 2003-11-10, under 510(k) number K032536.

Who is the listed applicant for SOMATOM EXTENDED FIELD OF VIEW SOFTWARE OPTION?

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 EXTENDED FIELD OF VIEW SOFTWARE OPTION?

The FDA product code for SOMATOM EXTENDED FIELD OF VIEW SOFTWARE OPTION 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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