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FDA 510(k)

NEUROCOMP

K-Number: K993654 · 2000-01-27

ApplicantNeurocybernetics
Decision Date2000-01-27
Product CodeHCC
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NEUROCOMP is the device name listed in this FDA 510(k) record. The listed applicant is Neurocybernetics. It received FDA 510(k) clearance on 2000-01-27 under 510(k) number K993654. The device is classified under product code HCC. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEUROCOMP?

NEUROCOMP is a medical device that received FDA 510(k) clearance on 2000-01-27. The listed applicant is Neurocybernetics. The 510(k) number is K993654.

When did NEUROCOMP receive FDA 510(k) clearance?

NEUROCOMP received FDA 510(k) clearance on 2000-01-27, under 510(k) number K993654.

Who is the listed applicant for NEUROCOMP?

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

What is the FDA product code for NEUROCOMP?

The FDA product code for NEUROCOMP is HCC.

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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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