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FDA 510(k)

NMX-1000

K-Number: K040584 · 2004-04-22

ApplicantNeomedix Corp.
Decision Date2004-04-22
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

NMX-1000 is the device name listed in this FDA 510(k) record. The listed applicant is Neomedix Corp.. It received FDA 510(k) clearance on 2004-04-22 under 510(k) number K040584. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NMX-1000?

NMX-1000 is a medical device that received FDA 510(k) clearance on 2004-04-22. The listed applicant is Neomedix Corp.. The 510(k) number is K040584.

When did NMX-1000 receive FDA 510(k) clearance?

NMX-1000 received FDA 510(k) clearance on 2004-04-22, under 510(k) number K040584.

Who is the listed applicant for NMX-1000?

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

What is the FDA product code for NMX-1000?

The FDA product code for NMX-1000 is GEI.

Other records listing Neomedix Corp. as applicant

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.

K061258TRABECTOME HIGH FREQUENCY GENERATOR/LPK040239SUPRAFLOW CONSOLEK024304MICROSURGICAL BIPOLAR HANDPIECE

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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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