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FDA 510(k)

EpiLaze Multi-wavelength Laser

K-Number: K191162 · 2019-07-09

ApplicantRohrer Aesthetics, LLC
Decision Date2019-07-09
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

EpiLaze Multi-wavelength Laser is a medical device manufactured by Rohrer Aesthetics, LLC. It received FDA 510(k) clearance on 2019-07-09 under approval number K191162. The device is classified under product code GEX. It was reviewed by the SU advisory panel. Product code GEX falls under the category of Gastroenterology, which includes gastrointestinal diagnostic and therapeutic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EpiLaze Multi-wavelength Laser?

EpiLaze Multi-wavelength Laser is a medical device that received FDA 510(k) clearance on 2019-07-09. It is manufactured by Rohrer Aesthetics, LLC. The 510(k) number is K191162.

When was EpiLaze Multi-wavelength Laser approved by the FDA?

EpiLaze Multi-wavelength Laser received FDA 510(k) clearance on 2019-07-09, under approval number K191162.

What company makes EpiLaze Multi-wavelength Laser?

EpiLaze Multi-wavelength Laser is manufactured by Rohrer Aesthetics, LLC.

What is the FDA product code for EpiLaze Multi-wavelength Laser?

The FDA product code for EpiLaze Multi-wavelength Laser is GEX. This falls under the Gastroenterology category.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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