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FDA 510(k)

NEUROTECH RECOVERY

K-Number: K112934 · 2012-01-20

ApplicantBio-Medical Research, Ltd.
Decision Date2012-01-20
Product CodeGXY
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NEUROTECH RECOVERY is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Medical Research, Ltd.. It received FDA 510(k) clearance on 2012-01-20 under 510(k) number K112934. 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 NEUROTECH RECOVERY?

NEUROTECH RECOVERY is a medical device that received FDA 510(k) clearance on 2012-01-20. The listed applicant is Bio-Medical Research, Ltd.. The 510(k) number is K112934.

When did NEUROTECH RECOVERY receive FDA 510(k) clearance?

NEUROTECH RECOVERY received FDA 510(k) clearance on 2012-01-20, under 510(k) number K112934.

Who is the listed applicant for NEUROTECH RECOVERY?

The FDA 510(k) record lists Bio-Medical Research, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NEUROTECH RECOVERY?

The FDA product code for NEUROTECH RECOVERY is 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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