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FDA 510(k)

SONOCA 180/195 WOUND CARE SYSTEM

K-Number: K072904 · 2008-05-21

ApplicantSoering GmbH
Decision Date2008-05-21
Product CodeLFL
DecisionSubstantially Equivalent

Device Summary

SONOCA 180/195 WOUND CARE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Soering GmbH. It received FDA 510(k) clearance on 2008-05-21 under 510(k) number K072904. The device is classified under product code LFL. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SONOCA 180/195 WOUND CARE SYSTEM?

SONOCA 180/195 WOUND CARE SYSTEM is a medical device that received FDA 510(k) clearance on 2008-05-21. The listed applicant is Soering GmbH. The 510(k) number is K072904.

When did SONOCA 180/195 WOUND CARE SYSTEM receive FDA 510(k) clearance?

SONOCA 180/195 WOUND CARE SYSTEM received FDA 510(k) clearance on 2008-05-21, under 510(k) number K072904.

Who is the listed applicant for SONOCA 180/195 WOUND CARE SYSTEM?

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

What is the FDA product code for SONOCA 180/195 WOUND CARE SYSTEM?

The FDA product code for SONOCA 180/195 WOUND CARE SYSTEM is LFL.

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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.

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