PicoLO Nd: YAG Picosecond Laser System
K-Number: K203491 · 2021-04-07
Device Summary
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 2021-04-07. It is manufactured by Laseroptek Co., Ltd.. The 510(k) number is K203491.
When was PicoLO Nd: YAG Picosecond Laser System approved by the FDA?
PicoLO Nd: YAG Picosecond Laser System received FDA 510(k) clearance on 2021-04-07, under approval number K203491.
What company makes PicoLO Nd: YAG Picosecond Laser System?
PicoLO Nd: YAG Picosecond Laser System is manufactured by Laseroptek Co., Ltd..
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.
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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.