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FDA 510(k)

NEUROTECH KNEEHAB

K-Number: K024258 · 2005-03-04

ApplicantBio-Medical Research, Ltd.
Decision Date2005-03-04
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

NEUROTECH KNEEHAB 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 2005-03-04 under 510(k) number K024258. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEUROTECH KNEEHAB?

NEUROTECH KNEEHAB is a medical device that received FDA 510(k) clearance on 2005-03-04. The listed applicant is Bio-Medical Research, Ltd.. The 510(k) number is K024258.

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

NEUROTECH KNEEHAB received FDA 510(k) clearance on 2005-03-04, under 510(k) number K024258.

Who is the listed applicant for NEUROTECH KNEEHAB?

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 KNEEHAB?

The FDA product code for NEUROTECH KNEEHAB is IPF.

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Related Devices (Code: IPF)

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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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