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FDA 510(k)

SENO ADVANTAGE

K-Number: K033400 · 2003-12-04

ApplicantGe Medical Systems W-400
Decision Date2003-12-04
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SENO ADVANTAGE is the device name listed in this FDA 510(k) record. The listed applicant is Ge Medical Systems W-400. It received FDA 510(k) clearance on 2003-12-04 under 510(k) number K033400. 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 SENO ADVANTAGE?

SENO ADVANTAGE is a medical device that received FDA 510(k) clearance on 2003-12-04. The listed applicant is Ge Medical Systems W-400. The 510(k) number is K033400.

When did SENO ADVANTAGE receive FDA 510(k) clearance?

SENO ADVANTAGE received FDA 510(k) clearance on 2003-12-04, under 510(k) number K033400.

Who is the listed applicant for SENO ADVANTAGE?

The FDA 510(k) record lists Ge Medical Systems W-400 as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SENO ADVANTAGE?

The FDA product code for SENO ADVANTAGE 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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