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FDA 510(k)

TitanPico Laser Workstation (PICO-450)

K-Number: K233757 · 2024-04-11

Decision Date2024-04-11
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TitanPico Laser Workstation (PICO-450) is a medical device manufactured by Rhein Laser Technologies Co., Ltd.. It received FDA 510(k) clearance on 2024-04-11 under approval number K233757. 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 TitanPico Laser Workstation (PICO-450)?

TitanPico Laser Workstation (PICO-450) is a medical device that received FDA 510(k) clearance on 2024-04-11. It is manufactured by Rhein Laser Technologies Co., Ltd.. The 510(k) number is K233757.

When was TitanPico Laser Workstation (PICO-450) approved by the FDA?

TitanPico Laser Workstation (PICO-450) received FDA 510(k) clearance on 2024-04-11, under approval number K233757.

What company makes TitanPico Laser Workstation (PICO-450)?

TitanPico Laser Workstation (PICO-450) is manufactured by Rhein Laser Technologies Co., Ltd..

What is the FDA product code for TitanPico Laser Workstation (PICO-450)?

The FDA product code for TitanPico Laser Workstation (PICO-450) is GEX. This falls under the Gastroenterology category.

Other Devices by Rhein Laser Technologies Co., Ltd.

Related Devices (Code: GEX)

Official Source

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