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FDA 510(k)

SYNGO MI APPLICATIONS 2007A

K-Number: K063826 · 2007-01-12

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2007-01-12
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SYNGO MI APPLICATIONS 2007A 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 2007-01-12 under 510(k) number K063826. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYNGO MI APPLICATIONS 2007A?

SYNGO MI APPLICATIONS 2007A is a medical device that received FDA 510(k) clearance on 2007-01-12. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K063826.

When did SYNGO MI APPLICATIONS 2007A receive FDA 510(k) clearance?

SYNGO MI APPLICATIONS 2007A received FDA 510(k) clearance on 2007-01-12, under 510(k) number K063826.

Who is the listed applicant for SYNGO MI APPLICATIONS 2007A?

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 MI APPLICATIONS 2007A?

The FDA product code for SYNGO MI APPLICATIONS 2007A is LLZ.

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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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