FDA 510(k)

Bestqool LED 치료 장치 (LMK-001, LMK-004, LMK-005, LMK-006)

K-번호: K242789 · 2025-01-02

신청자Dongguan Laiguang Electronic Technology Co., Ltd.

결정일2025-01-02

제품 코드OHS

자문 위원회SU [원문이 제공되지 않았기 때문에 번역할 수 없습니다. 원문을 제공해 주시면 번역을 도와드리겠습니다.]

결정대체적으로 동일

기기 요약

Bestqool LED Therapy Device (LMK-001,LMK-004,LMK-005,LMK-006) is the device name listed in this FDA 510(k) record. The listed applicant is Dongguan Laiguang Electronic Technology Co., Ltd.. It received FDA 510(k) clearance on 2025-01-02 under 510(k) number K242789. The device is classified under product code OHS. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the Bestqool LED Therapy Device (LMK-001,LMK-004,LMK-005,LMK-006)?

Bestqool LED Therapy Device (LMK-001,LMK-004,LMK-005,LMK-006) is a medical device that received FDA 510(k) clearance on 2025-01-02. The listed applicant is Dongguan Laiguang Electronic Technology Co., Ltd.. The 510(k) number is K242789.

When did Bestqool LED Therapy Device (LMK-001,LMK-004,LMK-005,LMK-006) receive FDA 510(k) clearance?

Bestqool LED Therapy Device (LMK-001,LMK-004,LMK-005,LMK-006) received FDA 510(k) clearance on 2025-01-02, under 510(k) number K242789.

Who is the listed applicant for Bestqool LED Therapy Device (LMK-001,LMK-004,LMK-005,LMK-006)?

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

What is the FDA product code for Bestqool LED Therapy Device (LMK-001,LMK-004,LMK-005,LMK-006)?

The FDA product code for Bestqool LED Therapy Device (LMK-001,LMK-004,LMK-005,LMK-006) is OHS.

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Bestqool LED 치료 장치 (LMK-001, LMK-004, LMK-005, LMK-006)

기기 요약

자주 묻는 질문

관련 임상시험

관련 기기 (코드: OHS)

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