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FDA 510(k)

NAFD 100

K-Number: K020848 · 2002-09-23

ApplicantNeomatrix, LLC
Decision Date2002-09-23
Product CodeKNW
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

NAFD 100 is the device name listed in this FDA 510(k) record. The listed applicant is Neomatrix, LLC. It received FDA 510(k) clearance on 2002-09-23 under 510(k) number K020848. The device is classified under product code KNW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NAFD 100?

NAFD 100 is a medical device that received FDA 510(k) clearance on 2002-09-23. The listed applicant is Neomatrix, LLC. The 510(k) number is K020848.

When did NAFD 100 receive FDA 510(k) clearance?

NAFD 100 received FDA 510(k) clearance on 2002-09-23, under 510(k) number K020848.

Who is the listed applicant for NAFD 100?

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

What is the FDA product code for NAFD 100?

The FDA product code for NAFD 100 is KNW.

Related Devices (Code: KNW)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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