FDA 510(k)

Holmium Laser Therapeutic Apparatus (HZ-40)

K-번호: K253633 · 2026-01-24

신청자Guangzhou Potent Medical Equipment Joint-Stock Co., Ltd.

결정일2026-01-24

제품 코드GEX

자문 위원회SU

결정Substantially Equivalent

기기 요약

Holmium Laser Therapeutic Apparatus (HZ-40) is the device name listed in this FDA 510(k) record. The listed applicant is Guangzhou Potent Medical Equipment Joint-Stock Co., Ltd.. It received FDA 510(k) clearance on 2026-01-24 under 510(k) number K253633. 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.

자주 묻는 질문

What is the Holmium Laser Therapeutic Apparatus (HZ-40)?

Holmium Laser Therapeutic Apparatus (HZ-40) is a medical device that received FDA 510(k) clearance on 2026-01-24. The listed applicant is Guangzhou Potent Medical Equipment Joint-Stock Co., Ltd.. The 510(k) number is K253633.

When did Holmium Laser Therapeutic Apparatus (HZ-40) receive FDA 510(k) clearance?

Holmium Laser Therapeutic Apparatus (HZ-40) received FDA 510(k) clearance on 2026-01-24, under 510(k) number K253633.

Who is the listed applicant for Holmium Laser Therapeutic Apparatus (HZ-40)?

The FDA 510(k) record lists Guangzhou Potent Medical Equipment Joint-Stock Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Holmium Laser Therapeutic Apparatus (HZ-40)?

The FDA product code for Holmium Laser Therapeutic Apparatus (HZ-40) is GEX. This falls under the Gastroenterology category.

Guangzhou Potent Medical Equipment Joint-Stock Co., Ltd.를 신청인으로 등재한 기타 기록

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