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FDA 510(k)

Stellar M22 for Intense Pulsed Light (IPL) and Laser System

K-Number: K193500 · 2020-01-16

ApplicantLumenis, Ltd.
Decision Date2020-01-16
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Stellar M22 for Intense Pulsed Light (IPL) and Laser System is a medical device manufactured by Lumenis, Ltd.. It received FDA 510(k) clearance on 2020-01-16 under approval number K193500. 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 Stellar M22 for Intense Pulsed Light (IPL) and Laser System?

Stellar M22 for Intense Pulsed Light (IPL) and Laser System is a medical device that received FDA 510(k) clearance on 2020-01-16. It is manufactured by Lumenis, Ltd.. The 510(k) number is K193500.

When was Stellar M22 for Intense Pulsed Light (IPL) and Laser System approved by the FDA?

Stellar M22 for Intense Pulsed Light (IPL) and Laser System received FDA 510(k) clearance on 2020-01-16, under approval number K193500.

What company makes Stellar M22 for Intense Pulsed Light (IPL) and Laser System?

Stellar M22 for Intense Pulsed Light (IPL) and Laser System is manufactured by Lumenis, Ltd..

What is the FDA product code for Stellar M22 for Intense Pulsed Light (IPL) and Laser System?

The FDA product code for Stellar M22 for Intense Pulsed Light (IPL) and Laser System is GEX. This falls under the Gastroenterology category.

Related Clinical Trials

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Related PubMed Literature

PMID: 40407411 A data augmentation approach for an automatic speech recognition system using laser Doppler vibrometer technology. JASA express letters (2025)

Other Devices by Lumenis, Ltd.

K170179LightSheer Desire; LightSheer Desire Light; LightSheer Duet; LightSheer Infinity K170060M22 and ResurFx Systems K170121Lumenis Family of Holmium Surgical Lasers and Delivery Devices and Accessories K162837Smart Laser Indirect Ophthalmoscope (LIO); Laser delivery device for Lumenis Novus Spectra Laser System, Lumenis Vision One Laser System, and Lumenis Smart532™ Laser System K180597AcuPulse (previously called AcuPulse 30/40 ST); AcuPulse 40W G; AcuPulse DUO K203544UltraPulse Surgical and Aesthetic CO2 Laser System, Delivery Devices and Accessories

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Related Devices (Code: GEX)

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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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