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FDA 510(k)

MODEL EC9-4 TRANSDUCER

K-Number: K060879 · 2006-04-19

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2006-04-19
Product CodeITX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MODEL EC9-4 TRANSDUCER 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 2006-04-19 under 510(k) number K060879. The device is classified under product code ITX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL EC9-4 TRANSDUCER?

MODEL EC9-4 TRANSDUCER is a medical device that received FDA 510(k) clearance on 2006-04-19. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K060879.

When did MODEL EC9-4 TRANSDUCER receive FDA 510(k) clearance?

MODEL EC9-4 TRANSDUCER received FDA 510(k) clearance on 2006-04-19, under 510(k) number K060879.

Who is the listed applicant for MODEL EC9-4 TRANSDUCER?

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 MODEL EC9-4 TRANSDUCER?

The FDA product code for MODEL EC9-4 TRANSDUCER is ITX.

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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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