FDA 510(k)

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K-번호: K172543 · 2018-07-11

신청자Beijing Dongbo Dental Handpiece Co., Ltd.

결정일2018-07-11

제품 코드EFB

자문 위원회의료 장비 규제 텍스트 번역 DE [회사명]의 [제품명]은 미국 식품의약국(FDA)에 등록된 의료 장비로, 510(k) 신청을 통해 승인을 받았습니다. 이 제품은 PMA(Premarket Approval)를 받지 않았으며, NCT(National Clinical Trial) 등록 번호는 [NCT 번호]입니다. PMID(Publication Medical Identifier)은 [PMID 번호]입니다. 더 자세한 정보는 다음 URL을 참조하세요: [URL]

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기기 요약

High-speed Turbine Handpieces for Single Use is the device name listed in this FDA 510(k) record. The listed applicant is Beijing Dongbo Dental Handpiece Co., Ltd.. It received FDA 510(k) clearance on 2018-07-11 under 510(k) number K172543. The device is classified under product code EFB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the High-speed Turbine Handpieces for Single Use?

High-speed Turbine Handpieces for Single Use is a medical device that received FDA 510(k) clearance on 2018-07-11. The listed applicant is Beijing Dongbo Dental Handpiece Co., Ltd.. The 510(k) number is K172543.

When did High-speed Turbine Handpieces for Single Use receive FDA 510(k) clearance?

High-speed Turbine Handpieces for Single Use received FDA 510(k) clearance on 2018-07-11, under 510(k) number K172543.

Who is the listed applicant for High-speed Turbine Handpieces for Single Use?

The FDA 510(k) record lists Beijing Dongbo Dental Handpiece Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for High-speed Turbine Handpieces for Single Use?

The FDA product code for High-speed Turbine Handpieces for Single Use is EFB.

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