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FDA 510(k)

PicoLO Nd:YAG Picosecond Laser System

K-Number: K183392 · 2019-01-04

ApplicantLaseroptek Co., Ltd.
Decision Date2019-01-04
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PicoLO Nd:YAG Picosecond Laser System is the device name listed in this FDA 510(k) record. The listed applicant is Laseroptek Co., Ltd.. It received FDA 510(k) clearance on 2019-01-04 under 510(k) number K183392. 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 PicoLO Nd:YAG Picosecond Laser System?

PicoLO Nd:YAG Picosecond Laser System is a medical device that received FDA 510(k) clearance on 2019-01-04. The listed applicant is Laseroptek Co., Ltd.. The 510(k) number is K183392.

When did PicoLO Nd:YAG Picosecond Laser System receive FDA 510(k) clearance?

PicoLO Nd:YAG Picosecond Laser System received FDA 510(k) clearance on 2019-01-04, under 510(k) number K183392.

Who is the listed applicant for PicoLO Nd:YAG Picosecond Laser System?

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

What is the FDA product code for PicoLO Nd:YAG Picosecond Laser System?

The FDA product code for PicoLO Nd:YAG Picosecond Laser System is GEX. This falls under the Gastroenterology category.

Other records listing Laseroptek Co., Ltd. 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.

K243780HELIOS 785 Pico (1754V2)K230373HELIOS 785 PicoK223588PALLAS PremiumK212663HELIOS IV 785K212573PicoLO PremiumK203491PicoLO Nd: YAG Picosecond Laser System

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Related Devices (Code: GEX)

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.

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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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