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FDA 510(k)

CEREBRALOGIK- AEEG

K-Number: K131789 · 2013-12-27

ApplicantMennen Medical , Ltd.
Decision Date2013-12-27
Product CodeOMA
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

CEREBRALOGIK- AEEG is the device name listed in this FDA 510(k) record. The listed applicant is Mennen Medical , Ltd.. It received FDA 510(k) clearance on 2013-12-27 under 510(k) number K131789. The device is classified under product code OMA. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CEREBRALOGIK- AEEG?

CEREBRALOGIK- AEEG is a medical device that received FDA 510(k) clearance on 2013-12-27. The listed applicant is Mennen Medical , Ltd.. The 510(k) number is K131789.

When did CEREBRALOGIK- AEEG receive FDA 510(k) clearance?

CEREBRALOGIK- AEEG received FDA 510(k) clearance on 2013-12-27, under 510(k) number K131789.

Who is the listed applicant for CEREBRALOGIK- AEEG?

The FDA 510(k) record lists Mennen Medical , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CEREBRALOGIK- AEEG?

The FDA product code for CEREBRALOGIK- AEEG is OMA.

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Other records listing Mennen Medical , Ltd. 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.

K123792HORIZON XVU (FFR)K093766VITALOGIK 6000/6500K091165HORIZON XVUK083063BIS INTERFACE FOR VITALOGIK PATIENT MONITORSK081484HORIZON XVUK073140VITALOGIK MODEL 4000/4500

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Related Devices (Code: OMA)

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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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