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FDA 510(k)

NOBLES-LAI VIDEO IMAGING SYSTEM

K-Number: K940273 · 1995-05-22

Decision Date1995-05-22
Product CodeGWG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NOBLES-LAI VIDEO IMAGING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Visioneering, Inc.. It received FDA 510(k) clearance on 1995-05-22 under 510(k) number K940273. The device is classified under product code GWG. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NOBLES-LAI VIDEO IMAGING SYSTEM?

NOBLES-LAI VIDEO IMAGING SYSTEM is a medical device that received FDA 510(k) clearance on 1995-05-22. The listed applicant is Visioneering, Inc.. The 510(k) number is K940273.

When did NOBLES-LAI VIDEO IMAGING SYSTEM receive FDA 510(k) clearance?

NOBLES-LAI VIDEO IMAGING SYSTEM received FDA 510(k) clearance on 1995-05-22, under 510(k) number K940273.

Who is the listed applicant for NOBLES-LAI VIDEO IMAGING SYSTEM?

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

What is the FDA product code for NOBLES-LAI VIDEO IMAGING SYSTEM?

The FDA product code for NOBLES-LAI VIDEO IMAGING SYSTEM is GWG.

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: GWG)

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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