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FDA 510(k)

NEURONET

K-Number: K952294 · 1996-01-26

ApplicantComputational Diagnostics, Inc.
Decision Date1996-01-26
Product CodeGWF
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NEURONET is the device name listed in this FDA 510(k) record. The listed applicant is Computational Diagnostics, Inc.. It received FDA 510(k) clearance on 1996-01-26 under 510(k) number K952294. The device is classified under product code GWF. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEURONET?

NEURONET is a medical device that received FDA 510(k) clearance on 1996-01-26. The listed applicant is Computational Diagnostics, Inc.. The 510(k) number is K952294.

When did NEURONET receive FDA 510(k) clearance?

NEURONET received FDA 510(k) clearance on 1996-01-26, under 510(k) number K952294.

Who is the listed applicant for NEURONET?

The FDA 510(k) record lists Computational Diagnostics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NEURONET?

The FDA product code for NEURONET is GWF.

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Related Devices (Code: GWF)

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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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