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FDA 510(k)

NEURO EASE

K-Number: K831785 · 1983-06-30

ApplicantAndover Medical, Inc.
Decision Date1983-06-30
Product CodeGXY
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NEURO EASE is the device name listed in this FDA 510(k) record. The listed applicant is Andover Medical, Inc.. It received FDA 510(k) clearance on 1983-06-30 under 510(k) number K831785. The device is classified under product code GXY. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEURO EASE?

NEURO EASE is a medical device that received FDA 510(k) clearance on 1983-06-30. The listed applicant is Andover Medical, Inc.. The 510(k) number is K831785.

When did NEURO EASE receive FDA 510(k) clearance?

NEURO EASE received FDA 510(k) clearance on 1983-06-30, under 510(k) number K831785.

Who is the listed applicant for NEURO EASE?

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

What is the FDA product code for NEURO EASE?

The FDA product code for NEURO EASE is GXY.

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Related Devices (Code: GXY)

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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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