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FDA 510(k)

Vevazz LED

K-Number: K172111 · 2017-11-22

ApplicantVevazz, LLC
Decision Date2017-11-22
Product CodeOLI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Vevazz LED is the device name listed in this FDA 510(k) record. The listed applicant is Vevazz, LLC. It received FDA 510(k) clearance on 2017-11-22 under 510(k) number K172111. The device is classified under product code OLI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Vevazz LED?

Vevazz LED is a medical device that received FDA 510(k) clearance on 2017-11-22. The listed applicant is Vevazz, LLC. The 510(k) number is K172111.

When did Vevazz LED receive FDA 510(k) clearance?

Vevazz LED received FDA 510(k) clearance on 2017-11-22, under 510(k) number K172111.

Who is the listed applicant for Vevazz LED?

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

What is the FDA product code for Vevazz LED?

The FDA product code for Vevazz LED is OLI.

Other records listing Vevazz, LLC 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.

Related Devices (Code: OLI)

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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