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FDA 510(k)

KIMBA MINI

K-Number: K080349 · 2008-03-10

ApplicantSignus Medizintechnik GmbH
Decision Date2008-03-10
Product CodeMQP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

KIMBA MINI is the device name listed in this FDA 510(k) record. The listed applicant is Signus Medizintechnik GmbH. It received FDA 510(k) clearance on 2008-03-10 under 510(k) number K080349. The device is classified under product code MQP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KIMBA MINI?

KIMBA MINI is a medical device that received FDA 510(k) clearance on 2008-03-10. The listed applicant is Signus Medizintechnik GmbH. The 510(k) number is K080349.

When did KIMBA MINI receive FDA 510(k) clearance?

KIMBA MINI received FDA 510(k) clearance on 2008-03-10, under 510(k) number K080349.

Who is the listed applicant for KIMBA MINI?

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

What is the FDA product code for KIMBA MINI?

The FDA product code for KIMBA MINI is MQP.

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Other records listing Signus Medizintechnik GmbH as applicant

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Related Devices (Code: MQP)

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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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