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FDA 510(k)

NOMAD FROM DYNAMIS MOBILITY LTD.

K-Number: K040457 · 2004-05-19

Decision Date2004-05-19
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

NOMAD FROM DYNAMIS MOBILITY LTD. is the device name listed in this FDA 510(k) record. The listed applicant is Dynamis Mobility , Ltd.. It received FDA 510(k) clearance on 2004-05-19 under 510(k) number K040457. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NOMAD FROM DYNAMIS MOBILITY LTD.?

NOMAD FROM DYNAMIS MOBILITY LTD. is a medical device that received FDA 510(k) clearance on 2004-05-19. The listed applicant is Dynamis Mobility , Ltd.. The 510(k) number is K040457.

When did NOMAD FROM DYNAMIS MOBILITY LTD. receive FDA 510(k) clearance?

NOMAD FROM DYNAMIS MOBILITY LTD. received FDA 510(k) clearance on 2004-05-19, under 510(k) number K040457.

Who is the listed applicant for NOMAD FROM DYNAMIS MOBILITY LTD.?

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

What is the FDA product code for NOMAD FROM DYNAMIS MOBILITY LTD.?

The FDA product code for NOMAD FROM DYNAMIS MOBILITY LTD. is ITI.

Related Clinical Trials

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.

Related Devices (Code: ITI)

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.

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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