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FDA 510(k)

MBC SERIES

K-Number: K024059 · 2003-01-08

ApplicantSoring GmbH Medizintechnik
Decision Date2003-01-08
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MBC SERIES 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 2003-01-08 under 510(k) number K024059. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MBC SERIES?

MBC SERIES is a medical device that received FDA 510(k) clearance on 2003-01-08. The listed applicant is Soring GmbH Medizintechnik. The 510(k) number is K024059.

When did MBC SERIES receive FDA 510(k) clearance?

MBC SERIES received FDA 510(k) clearance on 2003-01-08, under 510(k) number K024059.

Who is the listed applicant for MBC SERIES?

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 MBC SERIES?

The FDA product code for MBC SERIES is GEI.

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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/BCC140K052183SORING GMBH SONOCA LIPOK030028CPC BY SORING GMBHK012753SORING GMBH SONOCA 180/190K993265SORING GMBH, ARCO 3000, ARCO 2000, ARCO 1000, MBC 601, MBC 600K992026SORING GMBH, SONOCA 300

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Related Devices (Code: GEI)

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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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