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FDA 510(k)

Q-Switched Nd:Yag laser

K-Number: K232716 · 2023-11-30

ApplicantHebei Zhemai Technology Co., Ltd.
Decision Date2023-11-30
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Q-Switched Nd:Yag laser is the device name listed in this FDA 510(k) record. The listed applicant is Hebei Zhemai Technology Co., Ltd.. It received FDA 510(k) clearance on 2023-11-30 under 510(k) number K232716. 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 Q-Switched Nd:Yag laser?

Q-Switched Nd:Yag laser is a medical device that received FDA 510(k) clearance on 2023-11-30. The listed applicant is Hebei Zhemai Technology Co., Ltd.. The 510(k) number is K232716.

When did Q-Switched Nd:Yag laser receive FDA 510(k) clearance?

Q-Switched Nd:Yag laser received FDA 510(k) clearance on 2023-11-30, under 510(k) number K232716.

Who is the listed applicant for Q-Switched Nd:Yag laser?

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

What is the FDA product code for Q-Switched Nd:Yag laser?

The FDA product code for Q-Switched Nd:Yag laser is GEX. This falls under the Gastroenterology category.

Other records listing Hebei Zhemai Technology 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.

K232708Intense pulsed light therapy deviceK232709Diode laser therapy device

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.

K261841Q Switched Nd:YAG Laser machine (QLQW-01)Beijing Nubway S&T Co., Ltd.K261221SOLTIVE™ Laser System (SOLTIVE™ Pro SuperPulsed Laser, SOLTIVE™ Premium SuperPulsed Laser, SOLTIVE Laser Fibers, and Accessories)Olympus Surgical Technologies AmericaK261738Medical Thulium Fiber Laser Systems (UroFiber 150Q)Rhein Laser Technologies Co., Ltd.K261693Diode laser hair removal machine (QDTM-04)Beijing Nubway S&T Co., Ltd.K261674Skin Air Cooling System (QALF-01)Beijing Nubway S&T Co., Ltd.K261701Hemolase Fiber (Hemo-R-0.40-2.5/Hemo-R-0.60-2.5/Hemo-R-0.40-1.8/Hemo-R-0.60-1.8)Micro-Energy Medical Technology Co., Ltd.

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.

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