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FDA 510(k)

NUVO VERDE LED LIGHTING SYSTEM

K-Number: K083323 · 2009-01-28

ApplicantNuvo, Inc.
Decision Date2009-01-28
Product CodeFSY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

NUVO VERDE LED LIGHTING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Nuvo, Inc.. It received FDA 510(k) clearance on 2009-01-28 under 510(k) number K083323. The device is classified under product code FSY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NUVO VERDE LED LIGHTING SYSTEM?

NUVO VERDE LED LIGHTING SYSTEM is a medical device that received FDA 510(k) clearance on 2009-01-28. The listed applicant is Nuvo, Inc.. The 510(k) number is K083323.

When did NUVO VERDE LED LIGHTING SYSTEM receive FDA 510(k) clearance?

NUVO VERDE LED LIGHTING SYSTEM received FDA 510(k) clearance on 2009-01-28, under 510(k) number K083323.

Who is the listed applicant for NUVO VERDE LED LIGHTING SYSTEM?

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

What is the FDA product code for NUVO VERDE LED LIGHTING SYSTEM?

The FDA product code for NUVO VERDE LED LIGHTING SYSTEM is FSY.

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: FSY)

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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