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FDA 510(k)

SORING GMBH SONOCA LIPO

K-Number: K052183 · 2005-10-07

ApplicantSoring GmbH Medizintechnik
Decision Date2005-10-07
Product CodeQPB
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SORING GMBH SONOCA LIPO is the device name listed in this FDA 510(k) record. The listed applicant is Soring GmbH Medizintechnik. It received FDA 510(k) clearance on 2005-10-07 under 510(k) number K052183. The device is classified under product code QPB. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SORING GMBH SONOCA LIPO?

SORING GMBH SONOCA LIPO is a medical device that received FDA 510(k) clearance on 2005-10-07. The listed applicant is Soring GmbH Medizintechnik. The 510(k) number is K052183.

When did SORING GMBH SONOCA LIPO receive FDA 510(k) clearance?

SORING GMBH SONOCA LIPO received FDA 510(k) clearance on 2005-10-07, under 510(k) number K052183.

Who is the listed applicant for SORING GMBH SONOCA LIPO?

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

What is the FDA product code for SORING GMBH SONOCA LIPO?

The FDA product code for SORING GMBH SONOCA LIPO is QPB.

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Other records listing Soring GmbH Medizintechnik as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K093511SORING MBC200/BCC140K030028CPC BY SORING GMBHK024059MBC SERIESK012753SORING GMBH SONOCA 180/190K993265SORING GMBH, ARCO 3000, ARCO 2000, ARCO 1000, MBC 601, MBC 600K992026SORING GMBH, SONOCA 300

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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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