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FDA 510(k)

NEUROTECH BAXOLVE TYPE 294

K-Number: K023913 · 2003-08-25

ApplicantBio-Medical Research, Ltd.
Decision Date2003-08-25
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NEUROTECH BAXOLVE TYPE 294 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 2003-08-25 under 510(k) number K023913. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEUROTECH BAXOLVE TYPE 294?

NEUROTECH BAXOLVE TYPE 294 is a medical device that received FDA 510(k) clearance on 2003-08-25. The listed applicant is Bio-Medical Research, Ltd.. The 510(k) number is K023913.

When did NEUROTECH BAXOLVE TYPE 294 receive FDA 510(k) clearance?

NEUROTECH BAXOLVE TYPE 294 received FDA 510(k) clearance on 2003-08-25, under 510(k) number K023913.

Who is the listed applicant for NEUROTECH BAXOLVE TYPE 294?

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 BAXOLVE TYPE 294?

The FDA product code for NEUROTECH BAXOLVE TYPE 294 is GZJ.

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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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