FDA 510(k)

SONOSENS

K-Number: K033193 · 2004-01-23

Decision Date2004-01-23

Product CodeNKI

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

SONOSENS is the device name listed in this FDA 510(k) record. The listed applicant is Friendly Sensors AG. It received FDA 510(k) clearance on 2004-01-23 under 510(k) number K033193. The device is classified under product code NKI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SONOSENS?

SONOSENS is a medical device that received FDA 510(k) clearance on 2004-01-23. The listed applicant is Friendly Sensors AG. The 510(k) number is K033193.

When did SONOSENS receive FDA 510(k) clearance?

SONOSENS received FDA 510(k) clearance on 2004-01-23, under 510(k) number K033193.

Who is the listed applicant for SONOSENS?

The FDA 510(k) record lists Friendly Sensors AG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SONOSENS?

The FDA product code for SONOSENS is NKI.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.