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FDA 510(k)

SORING GMBH, ARCO 3000, ARCO 2000, ARCO 1000, MBC 601, MBC 600

K-Number: K993265 · 1999-10-22

ApplicantSoring GmbH Medizintechnik
Decision Date1999-10-22
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SORING GMBH, ARCO 3000, ARCO 2000, ARCO 1000, MBC 601, MBC 600 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 1999-10-22 under 510(k) number K993265. 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 GMBH, ARCO 3000, ARCO 2000, ARCO 1000, MBC 601, MBC 600?

SORING GMBH, ARCO 3000, ARCO 2000, ARCO 1000, MBC 601, MBC 600 is a medical device that received FDA 510(k) clearance on 1999-10-22. The listed applicant is Soring GmbH Medizintechnik. The 510(k) number is K993265.

When did SORING GMBH, ARCO 3000, ARCO 2000, ARCO 1000, MBC 601, MBC 600 receive FDA 510(k) clearance?

SORING GMBH, ARCO 3000, ARCO 2000, ARCO 1000, MBC 601, MBC 600 received FDA 510(k) clearance on 1999-10-22, under 510(k) number K993265.

Who is the listed applicant for SORING GMBH, ARCO 3000, ARCO 2000, ARCO 1000, MBC 601, MBC 600?

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, ARCO 3000, ARCO 2000, ARCO 1000, MBC 601, MBC 600?

The FDA product code for SORING GMBH, ARCO 3000, ARCO 2000, ARCO 1000, MBC 601, MBC 600 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 GMBHK024059MBC SERIESK012753SORING GMBH SONOCA 180/190K992026SORING 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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