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FDA 510(k)

SORING MBC200/BCC140

K-Number: K093511 · 2010-04-16

ApplicantSoring GmbH Medizintechnik
Decision Date2010-04-16
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SORING MBC200/BCC140 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 2010-04-16 under 510(k) number K093511. 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 SORING MBC200/BCC140?

SORING MBC200/BCC140 is a medical device that received FDA 510(k) clearance on 2010-04-16. The listed applicant is Soring GmbH Medizintechnik. The 510(k) number is K093511.

When did SORING MBC200/BCC140 receive FDA 510(k) clearance?

SORING MBC200/BCC140 received FDA 510(k) clearance on 2010-04-16, under 510(k) number K093511.

Who is the listed applicant for SORING MBC200/BCC140?

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 MBC200/BCC140?

The FDA product code for SORING MBC200/BCC140 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.

K052183SORING GMBH SONOCA LIPOK030028CPC 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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