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FDA 510(k)

THE VENUS SYSTEM

K-Number: K880773 · 1988-08-18

ApplicantNeuroscientific Corp.
Decision Date1988-08-18
Product CodeGWL
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

THE VENUS SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Neuroscientific Corp.. It received FDA 510(k) clearance on 1988-08-18 under 510(k) number K880773. The device is classified under product code GWL. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE VENUS SYSTEM?

THE VENUS SYSTEM is a medical device that received FDA 510(k) clearance on 1988-08-18. The listed applicant is Neuroscientific Corp.. The 510(k) number is K880773.

When did THE VENUS SYSTEM receive FDA 510(k) clearance?

THE VENUS SYSTEM received FDA 510(k) clearance on 1988-08-18, under 510(k) number K880773.

Who is the listed applicant for THE VENUS SYSTEM?

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

What is the FDA product code for THE VENUS SYSTEM?

The FDA product code for THE VENUS SYSTEM is GWL.

Related Clinical Trials

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Other records listing Neuroscientific Corp. 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.

K881358PG CONSEN CONTRAST SENSITIVITY TESTING PROGRAM

Related Devices (Code: GWL)

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.

K243746Delphi AmplifierQuantalx NeroscienceK242832NExT Station; NExT Station AdvancedEb Neuro S.P.A.K242305BE Plus PRO, Neurotravel LIGHTEb Neuro S.P.A.K240646DreamClearSomnomed Technologies Inc., Doing Business AS RemwareK232210X-trodes System MX-TrodesK230148VlabDormotech Medical, Ltd.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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