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FDA 510(k)

NEURITOR 2001

K-Number: K902752 · 1990-12-04

ApplicantImexco General , Ltd.
Decision Date1990-12-04
Product CodeGWQ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NEURITOR 2001 is the device name listed in this FDA 510(k) record. The listed applicant is Imexco General , Ltd.. It received FDA 510(k) clearance on 1990-12-04 under 510(k) number K902752. The device is classified under product code GWQ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEURITOR 2001?

NEURITOR 2001 is a medical device that received FDA 510(k) clearance on 1990-12-04. The listed applicant is Imexco General , Ltd.. The 510(k) number is K902752.

When did NEURITOR 2001 receive FDA 510(k) clearance?

NEURITOR 2001 received FDA 510(k) clearance on 1990-12-04, under 510(k) number K902752.

Who is the listed applicant for NEURITOR 2001?

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

What is the FDA product code for NEURITOR 2001?

The FDA product code for NEURITOR 2001 is GWQ.

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Related Devices (Code: GWQ)

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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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