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FDA 510(k)

NEMUS SYSTEM; NEMUS PC PERIPHERAL

K-Number: K073415 · 2008-05-23

ApplicantEb Neuro S.P.A.
Decision Date2008-05-23
Product CodeIKN
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

NEMUS SYSTEM; NEMUS PC PERIPHERAL is the device name listed in this FDA 510(k) record. The listed applicant is Eb Neuro S.P.A.. It received FDA 510(k) clearance on 2008-05-23 under 510(k) number K073415. The device is classified under product code IKN. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEMUS SYSTEM; NEMUS PC PERIPHERAL?

NEMUS SYSTEM; NEMUS PC PERIPHERAL is a medical device that received FDA 510(k) clearance on 2008-05-23. The listed applicant is Eb Neuro S.P.A.. The 510(k) number is K073415.

When did NEMUS SYSTEM; NEMUS PC PERIPHERAL receive FDA 510(k) clearance?

NEMUS SYSTEM; NEMUS PC PERIPHERAL received FDA 510(k) clearance on 2008-05-23, under 510(k) number K073415.

Who is the listed applicant for NEMUS SYSTEM; NEMUS PC PERIPHERAL?

The FDA 510(k) record lists Eb Neuro S.P.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NEMUS SYSTEM; NEMUS PC PERIPHERAL?

The FDA product code for NEMUS SYSTEM; NEMUS PC PERIPHERAL is IKN.

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Other records listing Eb Neuro S.P.A. 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.

K242832NExT Station; NExT Station AdvancedK242305BE Plus PRO, Neurotravel LIGHTK121996BE PLUS LTM AMPLIFIER GWI AMPLIFIERK093728BE MICRO, TREAK061996SANDMAN POCKETK053606BE PLUS / AURA-LTM64 AMPLIFIER

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Related Devices (Code: IKN)

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.

K172743Natus VikingQuestNatus Neurology IncorporatedK163150ViMove2Dorsavi, Ltd.K162383Cadwell Sierra Summit, Cadwell Sierra AscentCadwell Industries, Inc.K123902PHYSICAL MONITORING REGISTRATION UNIT-S (PMRU-S)Oktx, LLCK123399MYOVISION 3.0 WIREFREE SYSTEMPrecision Biometrics, Inc.K113074CMAP PROMedical Technologies, Inc.

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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