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FDA 510(k)

NOMAD ND1000M AUGMENTED VISION SYSTEM

K-Number: K030940 · 2003-04-09

ApplicantMicrovision Incorporated
Decision Date2003-04-09
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

NOMAD ND1000M AUGMENTED VISION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Microvision Incorporated. It received FDA 510(k) clearance on 2003-04-09 under 510(k) number K030940. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NOMAD ND1000M AUGMENTED VISION SYSTEM?

NOMAD ND1000M AUGMENTED VISION SYSTEM is a medical device that received FDA 510(k) clearance on 2003-04-09. The listed applicant is Microvision Incorporated. The 510(k) number is K030940.

When did NOMAD ND1000M AUGMENTED VISION SYSTEM receive FDA 510(k) clearance?

NOMAD ND1000M AUGMENTED VISION SYSTEM received FDA 510(k) clearance on 2003-04-09, under 510(k) number K030940.

Who is the listed applicant for NOMAD ND1000M AUGMENTED VISION SYSTEM?

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

What is the FDA product code for NOMAD ND1000M AUGMENTED VISION SYSTEM?

The FDA product code for NOMAD ND1000M AUGMENTED VISION SYSTEM is GCJ.

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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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